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FDA 510(k)

GO-CLEAN

K-Number: K922110 · 1994-03-09

ApplicantViva-Tek Assoc., Inc.
Decision Date1994-03-09
Product CodeFRR
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GO-CLEAN is the device name listed in this FDA 510(k) record. The listed applicant is Viva-Tek Assoc., Inc.. It received FDA 510(k) clearance on 1994-03-09 under 510(k) number K922110. The device is classified under product code FRR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GO-CLEAN?

GO-CLEAN is a medical device that received FDA 510(k) clearance on 1994-03-09. The listed applicant is Viva-Tek Assoc., Inc.. The 510(k) number is K922110.

When did GO-CLEAN receive FDA 510(k) clearance?

GO-CLEAN received FDA 510(k) clearance on 1994-03-09, under 510(k) number K922110.

Who is the listed applicant for GO-CLEAN?

The FDA 510(k) record lists Viva-Tek Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GO-CLEAN?

The FDA product code for GO-CLEAN is FRR.

Related Clinical Trials

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Other records listing Viva-Tek Assoc., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K920043AIRES

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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