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

Table, Operating-Room, Non-Electrical

21 CFR 878.4950 / General, Plastic Surgery
FDA source (opens on fda.gov)

FWY is the FDA product code for Table, Operating-Room, Non-Electrical, a class I device type, regulated under 21 CFR 878.4950. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FWY
Device name
Table, Operating-Room, Non-Electrical
Regulation
21 CFR 878.4950
Device class
Class I
Review panel
General, Plastic Surgery
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
4
Ingested recalls
0

Clearances, product code FWY

By decision year
4 clearances under product code FWY with a decision year between 1980 and 1988, 1980 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FWY by decision year
YearClearances
19801
19831
19871
19881

Applicants with the most clearances

Product code FWY
Applicants holding the most 510(k) clearances under product code FWY
ApplicantClearances
Mizuho Orthopedic Systems Inc1
Skytron, LLC1
Stryker Corp.1
Warner-Lambert Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code