FASTDAM— 510(k) K972775

Substantially Equivalent

Interdent, Inc.

FDA 510(k) clearance K972775 for FASTDAM, Substantially Equivalent on 1998-02-27. Applicant: Interdent, Inc.. Device class: 1.

Clearance details

Applicant: Interdent, Inc.
Product code: Code EIE
Device class: Class 1
Regulation: 21 CFR 872.6300
Advisory panel: Dental
Date received: 1997-07-24
Decision date: 1998-02-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, US

Download summary PDF View on FDA.gov ↗

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