OCCLUFAST
K-Number: K935889 · 1994-08-23
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Device Summary
Frequently Asked Questions
What is the OCCLUFAST?
OCCLUFAST is a medical device that received FDA 510(k) clearance on 1994-08-23. The listed applicant is Zhermack Dental Production. The 510(k) number is K935889.
When did OCCLUFAST receive FDA 510(k) clearance?
OCCLUFAST received FDA 510(k) clearance on 1994-08-23, under 510(k) number K935889.
Who is the listed applicant for OCCLUFAST?
The FDA 510(k) record lists Zhermack Dental Production as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OCCLUFAST?
The FDA product code for OCCLUFAST 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 Dental Production 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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