OPTIBLAST INTRAORAL SANDBLASTER— 510(k) K955573

Name: FDA 510(k) clearance K955573
Creator: U.S. Food and Drug Administration
Published: 1996-05-03

Substantially Equivalent

Buffalo Dental Mfg. Co., Inc.

FDA 510(k) clearance K955573 for OPTIBLAST INTRAORAL SANDBLASTER, Substantially Equivalent on 1996-05-03. Applicant: Buffalo Dental Mfg. Co., Inc.. Device class: 2.

Clearance details

Applicant: Buffalo Dental Mfg. Co., Inc.
Product code: Code KOJ
Device class: Class 2
Regulation: 21 CFR 872.6080
Advisory panel: Dental
Date received: 1995-12-07
Decision date: 1996-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Syosset, NY, US

Download summary PDF View on FDA.gov ↗

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