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FDA 510(k)

UTERINE DRESSING FORCEPS

K-Number: K890378 · 1989-02-13

Decision Date1989-02-13
Product CodeHCZ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

UTERINE DRESSING FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Kinetic Medical Products. It received FDA 510(k) clearance on 1989-02-13 under 510(k) number K890378. The device is classified under product code HCZ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UTERINE DRESSING FORCEPS?

UTERINE DRESSING FORCEPS is a medical device that received FDA 510(k) clearance on 1989-02-13. The listed applicant is Kinetic Medical Products. The 510(k) number is K890378.

When did UTERINE DRESSING FORCEPS receive FDA 510(k) clearance?

UTERINE DRESSING FORCEPS received FDA 510(k) clearance on 1989-02-13, under 510(k) number K890378.

Who is the listed applicant for UTERINE DRESSING FORCEPS?

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

What is the FDA product code for UTERINE DRESSING FORCEPS?

The FDA product code for UTERINE DRESSING FORCEPS is HCZ.

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 Kinetic Medical Products 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.

View all 63 devices →

Related Devices (Code: HCZ)

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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