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FDA 510(k)

CERCLAGE WIRE CRIMP BLOCK

K-Number: K960651 · 1996-05-03

ApplicantAcu-Med, Inc.
Decision Date1996-05-03
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CERCLAGE WIRE CRIMP BLOCK 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 1996-05-03 under 510(k) number K960651. 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 BLOCK?

CERCLAGE WIRE CRIMP BLOCK is a medical device that received FDA 510(k) clearance on 1996-05-03. The listed applicant is Acu-Med, Inc.. The 510(k) number is K960651.

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

CERCLAGE WIRE CRIMP BLOCK received FDA 510(k) clearance on 1996-05-03, under 510(k) number K960651.

Who is the listed applicant for CERCLAGE WIRE CRIMP BLOCK?

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 BLOCK?

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

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Other records listing Acu-Med, Inc. as applicant

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.

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Related Devices (Code: 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.

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