Atlas FDA

SURGICAL PREP RAZOR

FDA 510(k) clearance K874370 · decided 1987-11-13

Clearance details

K-number
K874370
Device name
SURGICAL PREP RAZOR
Applicant
Derma-Safe Co.
Decision
Substantially Equivalent
Date received
1987-10-26
Decision date
1987-11-13
Days to decision
18 days
Clearance type
Traditional
Product code
LWK
Device class
1
Regulation number
878.4800
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Wayne, NJ, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
3M(TM) SURGICAL SLIPPER, 9660 SERIES (K946162)Wahl Clipper Corp.1995-01-24
SURGICAL CLIPPER (K910524)Baxter Healthcare Corp1991-03-28
SURGICAL PREP RAZOR, STRAIGHT TYPE (K874234)Derma-Safe Co.1987-11-02

Recalls involving this device

No recalls on record reference this clearance.