Product code CCM— Anesthesiology
1085 ULTIMATE E PLETHYSMOGRAPH
- Classification name
- Plethysmograph, Pressure
- Device class
- Class 2
- Regulation
- 21 CFR 868.1750
- Advisory panel
- Anesthesiology
- Total cleared
- 11
- First cleared
- Most recent
Market context for product code CCM
FDA has cleared devices under product code CCM between 1978 and 2009, filed by 8 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
- 2009
- 2003
- 1995
- 1989
- 1986
- 1985
- 1979
- 1978
Top applicants under product code CCM
Recent clearances under product code CCM
- K081823 — MASTERSCREEN PAED - BABY BODY
- K023796 — MS PAED-BABY BODY
- K943259 — 1085 ULTIMATE E PLETHYSMOGRAPH
- K893420 — MASTERLAB PFT AND MASTERLAB BODY BOX
- K853390 — INFANT BODY TEST
- K852102 — COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEM
- K852088 — SYSTEM 1085 BODY PLETHYSMOGRAPH
- K843846 — UNIVERSAL-BODYTEST
- K843851 — BODYSCREEN II
- K791705 — 4200 PNEUMATIC MOUTH SHUTTER
- K772367 — CHEST BELLOWS, SMALL
Data sourced from openFDA. This site is unofficial and independent of the FDA.