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FDA 510(k)

RAZOR, SCHICK DISPOSABLE

K-Number: K760342 · 1976-08-11

ApplicantParke-Davis Co.
Decision Date1976-08-11
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RAZOR, SCHICK DISPOSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Parke-Davis Co.. It received FDA 510(k) clearance on 1976-08-11 under 510(k) number K760342. The device is classified under product code LDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAZOR, SCHICK DISPOSABLE?

RAZOR, SCHICK DISPOSABLE is a medical device that received FDA 510(k) clearance on 1976-08-11. The listed applicant is Parke-Davis Co.. The 510(k) number is K760342.

When did RAZOR, SCHICK DISPOSABLE receive FDA 510(k) clearance?

RAZOR, SCHICK DISPOSABLE received FDA 510(k) clearance on 1976-08-11, under 510(k) number K760342.

Who is the listed applicant for RAZOR, SCHICK DISPOSABLE?

The FDA 510(k) record lists Parke-Davis Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RAZOR, SCHICK DISPOSABLE?

The FDA product code for RAZOR, SCHICK DISPOSABLE is LDQ.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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