DeviceClearance

ADPHARMA OCCLUDE AND OCCLUDE F DENTIN TUBULE AGENT— 510(k) K082071

Substantially Equivalent

Adpharma, Inc.

FDA 510(k) clearance K082071 for ADPHARMA OCCLUDE AND OCCLUDE F DENTIN TUBULE AGENT, Substantially Equivalent on 2008-10-02. Applicant: Adpharma, Inc.. Device class: 2.

Clearance details

Applicant
Adpharma, Inc.
Product code
Code LBH
Device class
Class 2
Regulation
21 CFR 872.3260
Advisory panel
Dental
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Arlington Heights, IL, US
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