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FDA 510(k)

LUNEAU UMBILICAL CORD CLAMP

K-Number: K923439 · 1993-05-21

Decision Date1993-05-21
Product CodeHFW
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LUNEAU UMBILICAL CORD CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Laboratoires Luneau. It received FDA 510(k) clearance on 1993-05-21 under 510(k) number K923439. The device is classified under product code HFW. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUNEAU UMBILICAL CORD CLAMP?

LUNEAU UMBILICAL CORD CLAMP is a medical device that received FDA 510(k) clearance on 1993-05-21. The listed applicant is Laboratoires Luneau. The 510(k) number is K923439.

When did LUNEAU UMBILICAL CORD CLAMP receive FDA 510(k) clearance?

LUNEAU UMBILICAL CORD CLAMP received FDA 510(k) clearance on 1993-05-21, under 510(k) number K923439.

Who is the listed applicant for LUNEAU UMBILICAL CORD CLAMP?

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

What is the FDA product code for LUNEAU UMBILICAL CORD CLAMP?

The FDA product code for LUNEAU UMBILICAL CORD CLAMP is HFW.

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: HFW)

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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