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

Table, Operating-Room, Pneumatic

21 CFR 878.4960 / General, Plastic Surgery
FDA source (opens on fda.gov)

FWW is the FDA product code for Table, Operating-Room, Pneumatic, a class I device type, regulated under 21 CFR 878.4960. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
FWW
Device name
Table, Operating-Room, Pneumatic
Regulation
21 CFR 878.4960
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
6
Ingested recalls
0

Clearances, product code FWW

By decision year
6 clearances under product code FWW with a decision year between 1985 and 1995, 1993 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code FWW by decision year
YearClearances
19851
19861
19932
19941
19951

Applicants with the most clearances

Product code FWW
Applicants holding the most 510(k) clearances under product code FWW
ApplicantClearances
Amsco American Sterilizer Co.1
Kamiya Tsusan Kaisha, Ltd.1
Osteonics Corp.1
Skytron, LLC1
T. Korossurgical Instruments Corp.1
Vvortex International Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 13 companies shown, in name order