3M RESIN CEMENT— 510(k) K952121

Substantially Equivalent

3M Medical Products Group

FDA 510(k) clearance K952121 for 3M RESIN CEMENT, Substantially Equivalent on 1995-06-22. Applicant: 3M Medical Products Group. Device class: 2.

Clearance details

Applicant: 3M Medical Products Group
Product code: Code EMA
Device class: Class 2
Regulation: 21 CFR 872.3275
Advisory panel: Dental
Date received: 1995-05-05
Decision date: 1995-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.