POST CEMENT (DENTAL COMPOSITE)
K-Number: K902894 · 1990-08-01
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Device Summary
Frequently Asked Questions
What is the POST CEMENT (DENTAL COMPOSITE)?
POST CEMENT (DENTAL COMPOSITE) is a medical device that received FDA 510(k) clearance on 1990-08-01. The listed applicant is Medical Device Inspection Co., Inc.. The 510(k) number is K902894.
When did POST CEMENT (DENTAL COMPOSITE) receive FDA 510(k) clearance?
POST CEMENT (DENTAL COMPOSITE) received FDA 510(k) clearance on 1990-08-01, under 510(k) number K902894.
Who is the listed applicant for POST CEMENT (DENTAL COMPOSITE)?
The FDA 510(k) record lists Medical Device Inspection Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POST CEMENT (DENTAL COMPOSITE)?
The FDA product code for POST CEMENT (DENTAL COMPOSITE) is EMA.
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 Medical Device Inspection Co., Inc. 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: EMA)
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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