FDA 510(k)

EXPANSION COUPLER & MANUAL DRILL AS ACCESSORY SET

K-Number: K882286 · 1988-07-18

Decision Date1988-07-18

Product CodeGWM

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

EXPANSION COUPLER & MANUAL DRILL AS ACCESSORY SET is the device name listed in this FDA 510(k) record. The listed applicant is Metatech Corp.. It received FDA 510(k) clearance on 1988-07-18 under 510(k) number K882286. The device is classified under product code GWM. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXPANSION COUPLER & MANUAL DRILL AS ACCESSORY SET?

EXPANSION COUPLER & MANUAL DRILL AS ACCESSORY SET is a medical device that received FDA 510(k) clearance on 1988-07-18. The listed applicant is Metatech Corp.. The 510(k) number is K882286.

When did EXPANSION COUPLER & MANUAL DRILL AS ACCESSORY SET receive FDA 510(k) clearance?

EXPANSION COUPLER & MANUAL DRILL AS ACCESSORY SET received FDA 510(k) clearance on 1988-07-18, under 510(k) number K882286.

Who is the listed applicant for EXPANSION COUPLER & MANUAL DRILL AS ACCESSORY SET?

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

What is the FDA product code for EXPANSION COUPLER & MANUAL DRILL AS ACCESSORY SET?

The FDA product code for EXPANSION COUPLER & MANUAL DRILL AS ACCESSORY SET is GWM.

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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.