ENDODONTIC POST SYSTEMS
K-Number: K810977 · 1981-05-13
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Device Summary
Frequently Asked Questions
What is the ENDODONTIC POST SYSTEMS?
ENDODONTIC POST SYSTEMS is a medical device that received FDA 510(k) clearance on 1981-05-13. The listed applicant is Preat Corp.. The 510(k) number is K810977.
When did ENDODONTIC POST SYSTEMS receive FDA 510(k) clearance?
ENDODONTIC POST SYSTEMS received FDA 510(k) clearance on 1981-05-13, under 510(k) number K810977.
Who is the listed applicant for ENDODONTIC POST SYSTEMS?
The FDA 510(k) record lists Preat Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENDODONTIC POST SYSTEMS?
The FDA product code for ENDODONTIC POST SYSTEMS is ECG.
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: ECG)
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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