510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
LWKClass I

Razor, Surgical

21 CFR 878.4800 / General, Plastic Surgery
FDA source (opens on fda.gov)

LWK is the FDA product code for Razor, Surgical, a class I device type, regulated under 21 CFR 878.4800. As of , FDA records hold 4 510(k) clearances under this code, the most recent dated , and 6 recalls.

Classification record

Product code
LWK
Device name
Razor, Surgical
Regulation
21 CFR 878.4800
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
6

Clearances, product code LWK

By decision year
4 clearances under product code LWK with a decision year between 1987 and 1995, 1987 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code LWK by decision year
YearClearances
19872
19911
19951

Applicants with the most clearances

Product code LWK
Applicants holding the most 510(k) clearances under product code LWK
ApplicantClearances
Derma-Safe Co.2
Baxter Healthcare Corporation1
Wahl Clipper Corp1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 105 companies shown, in name order