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FDA 510(k)

ZEPPELIN FORCEPS

K-Number: K891047 · 1989-03-17

Decision Date1989-03-17
Product CodeHCZ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ZEPPELIN FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Zinnanti Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1989-03-17 under 510(k) number K891047. 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 ZEPPELIN FORCEPS?

ZEPPELIN FORCEPS is a medical device that received FDA 510(k) clearance on 1989-03-17. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K891047.

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

ZEPPELIN FORCEPS received FDA 510(k) clearance on 1989-03-17, under 510(k) number K891047.

Who is the listed applicant for ZEPPELIN FORCEPS?

The FDA 510(k) record lists Zinnanti Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ZEPPELIN FORCEPS?

The FDA product code for ZEPPELIN 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 Zinnanti Surgical Instruments, Inc. 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 76 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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