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FDA 510(k)

PERNECZKY CLIP APPLIER/REMOVER

K-Number: K954658 · 1996-10-08

Decision Date1996-10-08
Product CodeHCI
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PERNECZKY CLIP APPLIER/REMOVER is the device name listed in this FDA 510(k) record. The listed applicant is Von Zeppelin GmbH. It received FDA 510(k) clearance on 1996-10-08 under 510(k) number K954658. The device is classified under product code HCI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERNECZKY CLIP APPLIER/REMOVER?

PERNECZKY CLIP APPLIER/REMOVER is a medical device that received FDA 510(k) clearance on 1996-10-08. The listed applicant is Von Zeppelin GmbH. The 510(k) number is K954658.

When did PERNECZKY CLIP APPLIER/REMOVER receive FDA 510(k) clearance?

PERNECZKY CLIP APPLIER/REMOVER received FDA 510(k) clearance on 1996-10-08, under 510(k) number K954658.

Who is the listed applicant for PERNECZKY CLIP APPLIER/REMOVER?

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

What is the FDA product code for PERNECZKY CLIP APPLIER/REMOVER?

The FDA product code for PERNECZKY CLIP APPLIER/REMOVER is HCI.

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 Von Zeppelin GmbH 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.

Related Devices (Code: HCI)

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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