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FDA 510(k)

HYSTERECTOMY FORCEPS

K-Number: K926531 · 1994-02-25

Decision Date1994-02-25
Product CodeHCZ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

HYSTERECTOMY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Thomasville Medical Assoc.. It received FDA 510(k) clearance on 1994-02-25 under 510(k) number K926531. 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 HYSTERECTOMY FORCEPS?

HYSTERECTOMY FORCEPS is a medical device that received FDA 510(k) clearance on 1994-02-25. The listed applicant is Thomasville Medical Assoc.. The 510(k) number is K926531.

When did HYSTERECTOMY FORCEPS receive FDA 510(k) clearance?

HYSTERECTOMY FORCEPS received FDA 510(k) clearance on 1994-02-25, under 510(k) number K926531.

Who is the listed applicant for HYSTERECTOMY FORCEPS?

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

What is the FDA product code for HYSTERECTOMY FORCEPS?

The FDA product code for HYSTERECTOMY 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 Thomasville Medical Assoc. 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 33 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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