INTERJET(TM) GINGIVAL CARE INSTRUMENT— 510(k) K921999

Substantially Equivalent

Bausch & Lomb, Inc.

FDA 510(k) clearance K921999 for INTERJET(TM) GINGIVAL CARE INSTRUMENT, Substantially Equivalent on 1992-06-03. Applicant: Bausch & Lomb, Inc..

Clearance details

Applicant: Bausch & Lomb, Inc.
Product code: Code EFS
Advisory panel: Dental
Date received: 1992-04-29
Decision date: 1992-06-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tucker, GA, US

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