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FDA 510(k)

FORCEPS, OB, NON-COMPRESSIVE

K-Number: K771106 · 1977-07-01

Decision Date1977-07-01
Product CodeHDA
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FORCEPS, OB, NON-COMPRESSIVE is the device name listed in this FDA 510(k) record. The listed applicant is Zeppelin Medizinlechnik GmbH. It received FDA 510(k) clearance on 1977-07-01 under 510(k) number K771106. The device is classified under product code HDA. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORCEPS, OB, NON-COMPRESSIVE?

FORCEPS, OB, NON-COMPRESSIVE is a medical device that received FDA 510(k) clearance on 1977-07-01. The listed applicant is Zeppelin Medizinlechnik GmbH. The 510(k) number is K771106.

When did FORCEPS, OB, NON-COMPRESSIVE receive FDA 510(k) clearance?

FORCEPS, OB, NON-COMPRESSIVE received FDA 510(k) clearance on 1977-07-01, under 510(k) number K771106.

Who is the listed applicant for FORCEPS, OB, NON-COMPRESSIVE?

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

What is the FDA product code for FORCEPS, OB, NON-COMPRESSIVE?

The FDA product code for FORCEPS, OB, NON-COMPRESSIVE is HDA.

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: HDA)

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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