PERNECZKY CLIP APPLIER/REMOVER
K-Number: K954658 · 1996-10-08
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Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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