Product Code: OJW FDA class 2 21 CFR 878.4370

Shave Prep Kit

General, Plastic Surgery

The Shave Prep Kit is a convenience kit containing components used to shave and prepare a patient's surgical site prior to an operative procedure, typically including a razor and skin preparation materials to reduce hair at the incision area. Classified as FDA Class 2 under regulation 21 CFR 878.4370 within the General, Plastic Surgery medical specialty, it is under enforcement discretion per the FDA's May 1997 Convenience Kits Interim Regulatory Guidance and does not require a 510(k) when all applicable criteria are satisfied. The product code is OJW. It is not flagged as an implant or life-sustaining device.

510(k)s
0
FEI Numbers
11
Registration Numbers
11
Unique Applicants
0
Years Active

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Basic Information

Product Code
OJW
Device Class
FDA class 2
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Review Panel
SU
Submission Type
7

Device Characteristics

GMP Exempt
Implant
Life Sustain/Support
Third Party
Summary Malfunction Reporting

Definition

This product code has been established in accordance with the May 20, 1997, Guidance entitled, Convenience Kits Interim Regulatory Guidance, found at www.fda.gov/cdrh/ode/convkit.html. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.

FEI Numbers

This FDA classification entry is associated with 11 FEI numbers. Click on an entry to view related FDA registrations.

Registration Numbers

This FDA classification entry is associated with 11 registration numbers. Click on an entry to view related FDA registrations.