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FDA 510(k)

GRIDLOCK 195 ADHESIVE

K-Number: K020648 · 2002-05-01

ApplicantAllodex Systems
Decision Date2002-05-01
Product CodeDYH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GRIDLOCK 195 ADHESIVE is the device name listed in this FDA 510(k) record. The listed applicant is Allodex Systems. It received FDA 510(k) clearance on 2002-05-01 under 510(k) number K020648. The device is classified under product code DYH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRIDLOCK 195 ADHESIVE?

GRIDLOCK 195 ADHESIVE is a medical device that received FDA 510(k) clearance on 2002-05-01. The listed applicant is Allodex Systems. The 510(k) number is K020648.

When did GRIDLOCK 195 ADHESIVE receive FDA 510(k) clearance?

GRIDLOCK 195 ADHESIVE received FDA 510(k) clearance on 2002-05-01, under 510(k) number K020648.

Who is the listed applicant for GRIDLOCK 195 ADHESIVE?

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

What is the FDA product code for GRIDLOCK 195 ADHESIVE?

The FDA product code for GRIDLOCK 195 ADHESIVE is DYH.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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