OCCLUFAST ROCK
K-Number: K024034 · 2002-12-18
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Device Summary
Frequently Asked Questions
What is the OCCLUFAST ROCK?
OCCLUFAST ROCK is a medical device that received FDA 510(k) clearance on 2002-12-18. The listed applicant is Zhermack S.P.A.. The 510(k) number is K024034.
When did OCCLUFAST ROCK receive FDA 510(k) clearance?
OCCLUFAST ROCK received FDA 510(k) clearance on 2002-12-18, under 510(k) number K024034.
Who is the listed applicant for OCCLUFAST ROCK?
The FDA 510(k) record lists Zhermack S.P.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OCCLUFAST ROCK?
The FDA product code for OCCLUFAST ROCK is ELW.
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 Zhermack S.P.A. 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: ELW)
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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