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FDA 510(k)

BOOTY ENDOSCOPE WARMER

K-Number: K933515 · 1993-10-27

ApplicantT-Med, Inc.
Decision Date1993-10-27
Product CodeGCI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BOOTY ENDOSCOPE WARMER is the device name listed in this FDA 510(k) record. The listed applicant is T-Med, Inc.. It received FDA 510(k) clearance on 1993-10-27 under 510(k) number K933515. The device is classified under product code GCI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOOTY ENDOSCOPE WARMER?

BOOTY ENDOSCOPE WARMER is a medical device that received FDA 510(k) clearance on 1993-10-27. The listed applicant is T-Med, Inc.. The 510(k) number is K933515.

When did BOOTY ENDOSCOPE WARMER receive FDA 510(k) clearance?

BOOTY ENDOSCOPE WARMER received FDA 510(k) clearance on 1993-10-27, under 510(k) number K933515.

Who is the listed applicant for BOOTY ENDOSCOPE WARMER?

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

What is the FDA product code for BOOTY ENDOSCOPE WARMER?

The FDA product code for BOOTY ENDOSCOPE WARMER is GCI.

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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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