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FDA 510(k)

KEITH A-GAURD

K-Number: K915107 · 1992-02-11

ApplicantKbk Medical Products, Inc.
Decision Date1992-02-11
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

KEITH A-GAURD is the device name listed in this FDA 510(k) record. The listed applicant is Kbk Medical Products, Inc.. It received FDA 510(k) clearance on 1992-02-11 under 510(k) number K915107. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KEITH A-GAURD?

KEITH A-GAURD is a medical device that received FDA 510(k) clearance on 1992-02-11. The listed applicant is Kbk Medical Products, Inc.. The 510(k) number is K915107.

When did KEITH A-GAURD receive FDA 510(k) clearance?

KEITH A-GAURD received FDA 510(k) clearance on 1992-02-11, under 510(k) number K915107.

Who is the listed applicant for KEITH A-GAURD?

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

What is the FDA product code for KEITH A-GAURD?

The FDA product code for KEITH A-GAURD is LYY.

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Official Source

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