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FDA 510(k)

KEYMED KEY LIGHT

K-Number: K813133 · 1981-11-20

ApplicantKeymed, Inc.
Decision Date1981-11-20
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KEYMED KEY LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Keymed, Inc.. It received FDA 510(k) clearance on 1981-11-20 under 510(k) number K813133. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KEYMED KEY LIGHT?

KEYMED KEY LIGHT is a medical device that received FDA 510(k) clearance on 1981-11-20. The listed applicant is Keymed, Inc.. The 510(k) number is K813133.

When did KEYMED KEY LIGHT receive FDA 510(k) clearance?

KEYMED KEY LIGHT received FDA 510(k) clearance on 1981-11-20, under 510(k) number K813133.

Who is the listed applicant for KEYMED KEY LIGHT?

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 KEYMED KEY LIGHT?

The FDA product code for KEYMED KEY LIGHT is HET.

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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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