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

Board, Bed

21 CFR 880.6070 / General Hospital
FDA source (opens on fda.gov)

FPS is the FDA product code for Board, Bed, a class I device type, regulated under 21 CFR 880.6070. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and 4 recalls.

Classification record

Product code
FPS
Device name
Board, Bed
Regulation
21 CFR 880.6070
Device class
Class I
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
1
Ingested recalls
4

Clearances, product code FPS

By decision year
1 clearance under product code FPS with a decision year between 1978 and 1978, 1978 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FPS by decision year
YearClearances
19781

Applicants with the most clearances

Product code FPS
Applicants holding the most 510(k) clearances under product code FPS
ApplicantClearances
Zimmer GmbH1

Companies listing this code with FDA

Companies whose registered establishments list this code