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FDA 510(k)

KIMGUARD PROCEDURE TRAY

K-Number: K852203 · 1985-06-07

ApplicantKimberly-Clark Corp.
Decision Date1985-06-07
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

KIMGUARD PROCEDURE TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Kimberly-Clark Corp.. It received FDA 510(k) clearance on 1985-06-07 under 510(k) number K852203. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KIMGUARD PROCEDURE TRAY?

KIMGUARD PROCEDURE TRAY is a medical device that received FDA 510(k) clearance on 1985-06-07. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K852203.

When did KIMGUARD PROCEDURE TRAY receive FDA 510(k) clearance?

KIMGUARD PROCEDURE TRAY received FDA 510(k) clearance on 1985-06-07, under 510(k) number K852203.

Who is the listed applicant for KIMGUARD PROCEDURE TRAY?

The FDA 510(k) record lists Kimberly-Clark Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KIMGUARD PROCEDURE TRAY?

The FDA product code for KIMGUARD PROCEDURE TRAY is FRG.

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Related Devices (Code: FRG)

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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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