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FDA 510(k)

KEY MED LEEDS ENDOSCOPE DISINFECTOR

K-Number: K820152 · 1982-01-29

ApplicantKeymed, Inc.
Decision Date1982-01-29
Product CodeFEB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KEY MED LEEDS ENDOSCOPE DISINFECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Keymed, Inc.. It received FDA 510(k) clearance on 1982-01-29 under 510(k) number K820152. 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 LEEDS ENDOSCOPE DISINFECTOR?

KEY MED LEEDS ENDOSCOPE DISINFECTOR is a medical device that received FDA 510(k) clearance on 1982-01-29. The listed applicant is Keymed, Inc.. The 510(k) number is K820152.

When did KEY MED LEEDS ENDOSCOPE DISINFECTOR receive FDA 510(k) clearance?

KEY MED LEEDS ENDOSCOPE DISINFECTOR received FDA 510(k) clearance on 1982-01-29, under 510(k) number K820152.

Who is the listed applicant for KEY MED LEEDS ENDOSCOPE DISINFECTOR?

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 LEEDS ENDOSCOPE DISINFECTOR?

The FDA product code for KEY MED LEEDS ENDOSCOPE DISINFECTOR is FEB.

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Other records listing Keymed, Inc. as applicant

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Related Devices (Code: 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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