Product code IOQ— Physical Medicine
ADD-ON TO CRITICAL PATIENT CARE BED
- Classification name
- Bed, Flotation Therapy, Powered
- Device class
- Class 2
- Regulation
- 21 CFR 890.5170
- Advisory panel
- Physical Medicine
- Total cleared
- 57
- First cleared
- Most recent
Market context for product code IOQ
FDA has cleared devices under product code IOQ between 1977 and 2015, filed by 35 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
last 15 years- 2015
- 2013
- 1998
- 1997
- 1995
- 1994
- 1993
- 1992
- 1991
- 1990
- 1989
- 1988
- 1987
- 1986
- 1984
Top applicants under product code IOQ
Adverse events under product code IOQ
product code IOQ- Malfunction
- 676
- Other
- 5
- Total
- 681
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recent clearances under product code IOQ
- K143414 — Hill-Rom Wireless Connectivity Module
- K122473 — TOTALCARE SPOT TOTALCARE BARIATRIC TOTALCARE DUO TOATALCARE BED SYSTEM TOTALCARE DUO2
- K973624 — NURSE'S AID PATIENT ROTATION SYSTEM
- K970363 — HYDROTEC LOW AIR LOSS THERAPY BED
- K970364 — AIRTEC2 LOW AIR LOSS THERAPY BED
- K970636 — TOTALCARE., MODULAR THERAPY SYSTEM (MTS)
- K964873 — SILKAIR LOW AIRLOSS THERAPY
- K970295 — FLEXICAIR EXLIPSE PLUS
- K943433 — TOTAL CONTACT SEAT RIPPLE SYSTEM
- K951001 — FLEXICAIR EXLIPSE
- K945729 — DYNAMICAIRE(TM) SLEEP SURFACE, ZONEAIR(TM) SLEEP SURFACE
- K941610 — CLENSICAIR LOW AIRLOSS HYDROTHERAPY
- K940662 — I-5000
- K931594 — THERA-TURN CM-1000 MATTRESS OVERLAY SYSTEM
- K932480 — PRISM
- K926189 — ORTHODERM CONSUMMATE AIR THERAPY BED W/SCALE
- K925694 — MICROAIR PUP
- K926456 — MICROAIR TURN-Q
- K923977 — AKROTECH 4000
- K922973 — RESTCUE CC
- K922140 — ORTHODERM CONVERTIBLE II
- K921768 — HAZEL II
- K920382 — FLEXICAIR LOW AIRLOSS THERAPY UNIT
- K915671 — B.A.S.E. BELLOWS AIR SUPPORT EQUIPMENT
- K912854 — TURBO
- K914674 — MICROAIR 3500
- K914851 — CLA-1400 SYSTEM
- K912855 — HAZEL
- K910851 — TASSI MK3 (TURNAIR)
- K905126 — COMFORT-AIRE
- K905156 — BIO MEDX AIR FLOTATION SYSTEM
- K905053 — STAGE ZERO AIR FLOTATION BED
- K903659 — STAGE III
- K901890 — MARK IV FLOATATION THERAPY BED
- K901295 — PULMONAIR 40 PATIENT MANAGEMENT SYSTEM
- K894723 — SYSTEM 2500 MEDICAL WATERBED
- K894353 — ORTHODERM CONVERTIBLE
- K893801 — M.F.S. LOW AIR LOSS PULSATING BED
- K893614 — AEROMAT MRS-1000
- K893708 — FLUIDIZED AIR BED
- K890935 — SYSTEM 3000 FLUIDIZED AIR BED
- K882177 — ADD-ON TO CRITICAL PATIENT CARE BED
- K881843 — PEDIATRIC HOSPITAL BED
- K883192 — SMI 3000 AIRBED
- K882607 — ULTRAFLOTATION BED
- K882229 — AIR BED & FLOTATION DERMAGARD 800 & 900 SYSTEMS
- K880486 — DERMGARD SYSTEM 800 AND 900
- K875321 — MODIFIED ROTATION AIR FLUIDIZED BED/THE THERAPULSE
- K871614 — DECUB-I-CON 800 AND 900 SYSTEM
- K871368 — SCHELL C.A.P.P. BED MODEL NRS. 1268 + 1269
- K864232 — ROTATION AIR FLUIDIZED BED/DELTA
- K863047 — FLEXICAIR
- K840881 — WATER FLOATION BED 800/TC/H
- K840882 — HOME CARE WATER FLOTATION BED HC4/TC/H
- K840697 — CALM WATER FLOTATION HOSPITAL BED
- K832829 — NEO-FLOAT NEONATAL FLOTATION SYS & RHYT
- K771264 — FLOTATION THERAPY BED
Data sourced from openFDA. This site is unofficial and independent of the FDA.