510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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FSAClass I

Lift, Patient, Non-Ac-Powered

21 CFR 880.5510 / General Hospital
FDA source (opens on fda.gov)

FSA is the FDA product code for Lift, Patient, Non-Ac-Powered, a class I device type, regulated under 21 CFR 880.5510. As of , FDA records hold 13 510(k) clearances under this code, the most recent dated , and 141 recalls.

Classification record

Product code
FSA
Device name
Lift, Patient, Non-Ac-Powered
Regulation
21 CFR 880.5510
Device class
Class I
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
13
Ingested recalls
141

Clearances, product code FSA

By decision year
13 clearances under product code FSA with a decision year between 1978 and 1994, 1984 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code FSA by decision year
YearClearances
19781
19791
19811
19831
19843
19852
19861
19901
19931
19941

Applicants with the most clearances

Product code FSA
Applicants holding the most 510(k) clearances under product code FSA
ApplicantClearances
Setma, Inc.2
Anodyne1
Century Manufacturing Co.1
Corda Int'L Holiday, Inc.1
Dutton-Lainson Co.1
Invacare GmbH1
Madshus A/S1
Martin Pelvic Lift Co.1
Medi-Man Rehabilitation Products, Inc.1
Orthopedic Equipment Co., Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 195 companies shown, in name order