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FDA 510(k)

RAZOR, DISPOSABLE

K-Number: K760328 · 1976-08-11

ApplicantDevon Industries, Inc.
Decision Date1976-08-11
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RAZOR, DISPOSABLE is the device name listed in this FDA 510(k) record. The listed applicant is Devon Industries, Inc.. It received FDA 510(k) clearance on 1976-08-11 under 510(k) number K760328. 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, DISPOSABLE?

RAZOR, DISPOSABLE is a medical device that received FDA 510(k) clearance on 1976-08-11. The listed applicant is Devon Industries, Inc.. The 510(k) number is K760328.

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

RAZOR, DISPOSABLE received FDA 510(k) clearance on 1976-08-11, under 510(k) number K760328.

Who is the listed applicant for RAZOR, DISPOSABLE?

The FDA 510(k) record lists Devon Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RAZOR, DISPOSABLE?

The FDA product code for RAZOR, DISPOSABLE is LDQ.

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Other records listing Devon Industries, Inc. as applicant

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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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