SCOTCHPRIME CERAMIC PRIMER
K-Number: K853698 · 1985-11-14
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Device Summary
Frequently Asked Questions
What is the SCOTCHPRIME CERAMIC PRIMER?
SCOTCHPRIME CERAMIC PRIMER is a medical device that received FDA 510(k) clearance on 1985-11-14. The listed applicant is 3M Company. The 510(k) number is K853698.
When did SCOTCHPRIME CERAMIC PRIMER receive FDA 510(k) clearance?
SCOTCHPRIME CERAMIC PRIMER received FDA 510(k) clearance on 1985-11-14, under 510(k) number K853698.
Who is the listed applicant for SCOTCHPRIME CERAMIC PRIMER?
The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SCOTCHPRIME CERAMIC PRIMER?
The FDA product code for SCOTCHPRIME CERAMIC PRIMER is EIH.
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 3M Company 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: EIH)
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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