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FDA 510(k)

FINE SURGICAL CIRCUMCISION CLAMP

K-Number: K040052 · 2004-04-09

Decision Date2004-04-09
Product CodeHFX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FINE SURGICAL CIRCUMCISION CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Fine Surgical Instrument Corp.. It received FDA 510(k) clearance on 2004-04-09 under 510(k) number K040052. The device is classified under product code HFX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FINE SURGICAL CIRCUMCISION CLAMP?

FINE SURGICAL CIRCUMCISION CLAMP is a medical device that received FDA 510(k) clearance on 2004-04-09. The listed applicant is Fine Surgical Instrument Corp.. The 510(k) number is K040052.

When did FINE SURGICAL CIRCUMCISION CLAMP receive FDA 510(k) clearance?

FINE SURGICAL CIRCUMCISION CLAMP received FDA 510(k) clearance on 2004-04-09, under 510(k) number K040052.

Who is the listed applicant for FINE SURGICAL CIRCUMCISION CLAMP?

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

What is the FDA product code for FINE SURGICAL CIRCUMCISION CLAMP?

The FDA product code for FINE SURGICAL CIRCUMCISION CLAMP is HFX.

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.

Related Devices (Code: HFX)

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.

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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