FDA 510(k)

CERCLAGE WIRE CRIMP SLEEVE

K-Number: K931246 · 1994-02-22

Decision Date1994-02-22

Product CodeJDQ

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

CERCLAGE WIRE CRIMP SLEEVE is the device name listed in this FDA 510(k) record. The listed applicant is Acu Med, Inc.. It received FDA 510(k) clearance on 1994-02-22 under 510(k) number K931246. The device is classified under product code JDQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERCLAGE WIRE CRIMP SLEEVE?

CERCLAGE WIRE CRIMP SLEEVE is a medical device that received FDA 510(k) clearance on 1994-02-22. The listed applicant is Acu Med, Inc.. The 510(k) number is K931246.

When did CERCLAGE WIRE CRIMP SLEEVE receive FDA 510(k) clearance?

CERCLAGE WIRE CRIMP SLEEVE received FDA 510(k) clearance on 1994-02-22, under 510(k) number K931246.

Who is the listed applicant for CERCLAGE WIRE CRIMP SLEEVE?

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

What is the FDA product code for CERCLAGE WIRE CRIMP SLEEVE?

The FDA product code for CERCLAGE WIRE CRIMP SLEEVE is JDQ.

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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.