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FDA 510(k)

KEY-MED FIBRESCOPE DISINFECTION TROLLEY

K-Number: K810818 · 1981-04-08

ApplicantKeymed, Inc.
Decision Date1981-04-08
Product CodeFEB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KEY-MED FIBRESCOPE DISINFECTION TROLLEY is the device name listed in this FDA 510(k) record. The listed applicant is Keymed, Inc.. It received FDA 510(k) clearance on 1981-04-08 under 510(k) number K810818. The device is classified under product code FEB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KEY-MED FIBRESCOPE DISINFECTION TROLLEY?

KEY-MED FIBRESCOPE DISINFECTION TROLLEY is a medical device that received FDA 510(k) clearance on 1981-04-08. The listed applicant is Keymed, Inc.. The 510(k) number is K810818.

When did KEY-MED FIBRESCOPE DISINFECTION TROLLEY receive FDA 510(k) clearance?

KEY-MED FIBRESCOPE DISINFECTION TROLLEY received FDA 510(k) clearance on 1981-04-08, under 510(k) number K810818.

Who is the listed applicant for KEY-MED FIBRESCOPE DISINFECTION TROLLEY?

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

What is the FDA product code for KEY-MED FIBRESCOPE DISINFECTION TROLLEY?

The FDA product code for KEY-MED FIBRESCOPE DISINFECTION TROLLEY is FEB.

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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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