IMCOR DENTAL IMPLANT SYSTEM ACCESSORIES
K-Number: K982492 · 1998-10-15
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Device Summary
Frequently Asked Questions
What is the IMCOR DENTAL IMPLANT SYSTEM ACCESSORIES?
IMCOR DENTAL IMPLANT SYSTEM ACCESSORIES is a medical device that received FDA 510(k) clearance on 1998-10-15. The listed applicant is Imcor. The 510(k) number is K982492.
When did IMCOR DENTAL IMPLANT SYSTEM ACCESSORIES receive FDA 510(k) clearance?
IMCOR DENTAL IMPLANT SYSTEM ACCESSORIES received FDA 510(k) clearance on 1998-10-15, under 510(k) number K982492.
Who is the listed applicant for IMCOR DENTAL IMPLANT SYSTEM ACCESSORIES?
The FDA 510(k) record lists Imcor as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IMCOR DENTAL IMPLANT SYSTEM ACCESSORIES?
The FDA product code for IMCOR DENTAL IMPLANT SYSTEM ACCESSORIES is DZE.
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 Imcor 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: DZE)
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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