Product code FSA— General Hospital
ANOLIFT - PORTABLE & ANOLIFT - GANTRY
- Classification name
- Lift, Patient, Non-Ac-Powered
- Device class
- Class 1
- Regulation
- 21 CFR 880.5510
- Advisory panel
- General Hospital
- Total cleared
- 13
- First cleared
- Most recent
Market context for product code FSA
FDA has cleared devices under product code FSA between 1978 and 1994, filed by 12 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1994
- 1993
- 1990
- 1986
- 1985
- 1984
- 1983
- 1981
- 1979
- 1978
Top applicants under product code FSA
Adverse events under product code FSA
product code FSA- Death
- 101
- Injury
- 767
- Malfunction
- 1,173
- Other
- 1
- Total
- 2,042
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 FSA
- K942807 — SURGICAL LIFT SHEET
- K930625 — SANITAS PATIENT LIFT
- K902141 — ANOLIFT - PORTABLE & ANOLIFT - GANTRY
- K860837 — HOYER ONE-TOUCH POWER LIFTER
- K851844 — MOLIFT
- K844976 — MEDI-MAN WATER POWERED BATH LIFT & HYDRAULIC LIFT
- K841395 — SHOWER TROLLEY
- K841398 — VARIABLE HEIGHT TRANSFER CHAIR
- K840997 — BATTERY POWERED PATIENT LIFT
- K823206 — MARTIN PELVIC LIFT
- K811899 — CENTURY LIFT TRANSFER SYSTEM
- K792601 — LIFELIFT MODELS ONE AND TWO
- K780684 — PATIENT LIFT
Data sourced from openFDA. This site is unofficial and independent of the FDA.