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FDA 510(k)

BLADE, SURGICAL PREP RAZOR STRAIGHT

K-Number: K880048 · 1988-03-04

ApplicantCrescent Corp.
Decision Date1988-03-04
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BLADE, SURGICAL PREP RAZOR STRAIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Crescent Corp.. It received FDA 510(k) clearance on 1988-03-04 under 510(k) number K880048. 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 BLADE, SURGICAL PREP RAZOR STRAIGHT?

BLADE, SURGICAL PREP RAZOR STRAIGHT is a medical device that received FDA 510(k) clearance on 1988-03-04. The listed applicant is Crescent Corp.. The 510(k) number is K880048.

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

BLADE, SURGICAL PREP RAZOR STRAIGHT received FDA 510(k) clearance on 1988-03-04, under 510(k) number K880048.

Who is the listed applicant for BLADE, SURGICAL PREP RAZOR STRAIGHT?

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

What is the FDA product code for BLADE, SURGICAL PREP RAZOR STRAIGHT?

The FDA product code for BLADE, SURGICAL PREP RAZOR STRAIGHT 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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