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FDA 510(k)

PERCUGUARD

K-Number: K992539 · 2000-02-18

ApplicantDigit-Pro
Decision Date2000-02-18
Product CodeLZB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PERCUGUARD is the device name listed in this FDA 510(k) record. The listed applicant is Digit-Pro. It received FDA 510(k) clearance on 2000-02-18 under 510(k) number K992539. The device is classified under product code LZB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERCUGUARD?

PERCUGUARD is a medical device that received FDA 510(k) clearance on 2000-02-18. The listed applicant is Digit-Pro. The 510(k) number is K992539.

When did PERCUGUARD receive FDA 510(k) clearance?

PERCUGUARD received FDA 510(k) clearance on 2000-02-18, under 510(k) number K992539.

Who is the listed applicant for PERCUGUARD?

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

What is the FDA product code for PERCUGUARD?

The FDA product code for PERCUGUARD is LZB.

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Related Devices (Code: LZB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K052387ARTHREX FINGERSHIELD FINGER GUARD, MODEL AR-7199-XXArthrex, Inc.K980827LATEX FINGER COT, POWDER-FREE, WITH PROTEIN LABELINGTucker & AssociatesK912042BETHEL PLUS MULTIPLE NAMESBethel Latex Products, Inc.K903073LATEX FINGER COTSDongkuk Trading Co., Ltd.

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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