SCOTCHBOND DENTAL ADHESIVE
K-Number: K813180 · 1982-01-12
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Device Summary
Frequently Asked Questions
What is the SCOTCHBOND DENTAL ADHESIVE?
SCOTCHBOND DENTAL ADHESIVE is a medical device that received FDA 510(k) clearance on 1982-01-12. The listed applicant is 3M Company. The 510(k) number is K813180.
When did SCOTCHBOND DENTAL ADHESIVE receive FDA 510(k) clearance?
SCOTCHBOND DENTAL ADHESIVE received FDA 510(k) clearance on 1982-01-12, under 510(k) number K813180.
Who is the listed applicant for SCOTCHBOND DENTAL ADHESIVE?
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 SCOTCHBOND DENTAL ADHESIVE?
The FDA product code for SCOTCHBOND DENTAL ADHESIVE is KLE.
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: KLE)
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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