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FDA 510(k)

ZZIPP INSTANT BOVIE CLEANER

K-Number: K900714 · 1990-03-27

Decision Date1990-03-27
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ZZIPP INSTANT BOVIE CLEANER is the device name listed in this FDA 510(k) record. The listed applicant is Grieshaber & Co.. It received FDA 510(k) clearance on 1990-03-27 under 510(k) number K900714. 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 ZZIPP INSTANT BOVIE CLEANER?

ZZIPP INSTANT BOVIE CLEANER is a medical device that received FDA 510(k) clearance on 1990-03-27. The listed applicant is Grieshaber & Co.. The 510(k) number is K900714.

When did ZZIPP INSTANT BOVIE CLEANER receive FDA 510(k) clearance?

ZZIPP INSTANT BOVIE CLEANER received FDA 510(k) clearance on 1990-03-27, under 510(k) number K900714.

Who is the listed applicant for ZZIPP INSTANT BOVIE CLEANER?

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

What is the FDA product code for ZZIPP INSTANT BOVIE CLEANER?

The FDA product code for ZZIPP INSTANT BOVIE CLEANER is GEI.

Related Clinical Trials

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.

Other records listing Grieshaber & Co. 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.

View all 15 devices →

Related Devices (Code: GEI)

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.

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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