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FDA 510(k)

CURETTE SET, ANTRUM, COAKLEY

K-Number: K872609 · 1987-07-15

Decision Date1987-07-15
Product CodeKAP
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

CURETTE SET, ANTRUM, COAKLEY is the device name listed in this FDA 510(k) record. The listed applicant is Military Engineering, Inc.. It received FDA 510(k) clearance on 1987-07-15 under 510(k) number K872609. The device is classified under product code KAP. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CURETTE SET, ANTRUM, COAKLEY?

CURETTE SET, ANTRUM, COAKLEY is a medical device that received FDA 510(k) clearance on 1987-07-15. The listed applicant is Military Engineering, Inc.. The 510(k) number is K872609.

When did CURETTE SET, ANTRUM, COAKLEY receive FDA 510(k) clearance?

CURETTE SET, ANTRUM, COAKLEY received FDA 510(k) clearance on 1987-07-15, under 510(k) number K872609.

Who is the listed applicant for CURETTE SET, ANTRUM, COAKLEY?

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

What is the FDA product code for CURETTE SET, ANTRUM, COAKLEY?

The FDA product code for CURETTE SET, ANTRUM, COAKLEY is KAP.

Related Clinical Trials

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.

Other records listing Military Engineering, 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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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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