FDA 510(k)

Fetzer Medical Gynecological Forceps

K-Number: K172661 · 2018-05-08

Decision Date2018-05-08

Product CodeHCZ

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

Fetzer Medical Gynecological Forceps is the device name listed in this FDA 510(k) record. The listed applicant is Fetzer Medical GmbH & Co. KG. It received FDA 510(k) clearance on 2018-05-08 under 510(k) number K172661. 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 Fetzer Medical Gynecological Forceps?

Fetzer Medical Gynecological Forceps is a medical device that received FDA 510(k) clearance on 2018-05-08. The listed applicant is Fetzer Medical GmbH & Co. KG. The 510(k) number is K172661.

When did Fetzer Medical Gynecological Forceps receive FDA 510(k) clearance?

Fetzer Medical Gynecological Forceps received FDA 510(k) clearance on 2018-05-08, under 510(k) number K172661.

Who is the listed applicant for Fetzer Medical Gynecological Forceps?

The FDA 510(k) record lists Fetzer Medical GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Fetzer Medical Gynecological Forceps?

The FDA product code for Fetzer Medical Gynecological Forceps is HCZ.

Other records listing Fetzer Medical GmbH & Co. KG 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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