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FDA 510(k)

SURGICAL PREP RAZOR

K-Number: K781437 · 1978-12-05

ApplicantWarren J. Grosjean
Decision Date1978-12-05
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SURGICAL PREP RAZOR is the device name listed in this FDA 510(k) record. The listed applicant is Warren J. Grosjean. It received FDA 510(k) clearance on 1978-12-05 under 510(k) number K781437. 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 SURGICAL PREP RAZOR?

SURGICAL PREP RAZOR is a medical device that received FDA 510(k) clearance on 1978-12-05. The listed applicant is Warren J. Grosjean. The 510(k) number is K781437.

When did SURGICAL PREP RAZOR receive FDA 510(k) clearance?

SURGICAL PREP RAZOR received FDA 510(k) clearance on 1978-12-05, under 510(k) number K781437.

Who is the listed applicant for SURGICAL PREP RAZOR?

The FDA 510(k) record lists Warren J. Grosjean as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGICAL PREP RAZOR?

The FDA product code for SURGICAL PREP RAZOR is LDQ.

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Official Source

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

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