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FDA 510(k)

CLEANCUT

K-Number: K972335 · 1999-01-07

ApplicantMedquest Products, Inc.
Decision Date1999-01-07
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CLEANCUT is the device name listed in this FDA 510(k) record. The listed applicant is Medquest Products, Inc.. It received FDA 510(k) clearance on 1999-01-07 under 510(k) number K972335. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEANCUT?

CLEANCUT is a medical device that received FDA 510(k) clearance on 1999-01-07. The listed applicant is Medquest Products, Inc.. The 510(k) number is K972335.

When did CLEANCUT receive FDA 510(k) clearance?

CLEANCUT received FDA 510(k) clearance on 1999-01-07, under 510(k) number K972335.

Who is the listed applicant for CLEANCUT?

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

What is the FDA product code for CLEANCUT?

The FDA product code for CLEANCUT is GEI.

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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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