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510(k) K874234

Device
SURGICAL PREP RAZOR, STRAIGHT TYPE
Applicant
DERMA-SAFE CO.
510(k) number
K874234
Product code
LWK  
Decision
Substantially Equivalent (SESE)
Decision date
1987-11-02
Date received
1987-10-15
Regulation
878.4800
Classification name
Razor, Surgical
Medical specialty
General & Plastic Surgery
Review panel
General & Plastic Surgery
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
WARREN J GROSJEAN
Address
32 Juniper Rd. Wayne NJ US 07470 07470

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code LWK  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K9461623M(TM) SURGICAL SLIPPER, 9660 SERIESWahl Clipper Corp.1995-01-24
K910524SURGICAL CLIPPERBaxter Healthcare Corp1991-03-28
K874370SURGICAL PREP RAZORDerma-Safe Co.1987-11-13

Legacy Summary#

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FDA Review#

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