INTERJET(TM) GINGIVAL CARE INSTRUMENT— 510(k) K921999
Substantially EquivalentBausch & Lomb, Inc.
FDA 510(k) clearance K921999 for INTERJET(TM) GINGIVAL CARE INSTRUMENT, Substantially Equivalent on 1992-06-03. Applicant: Bausch & Lomb, Inc.. Device class: 1.
Clearance details
- Applicant
- Bausch & Lomb, Inc.
- Product code
- Code EFS
- Device class
- Class 1
- Regulation
- 21 CFR 872.6510
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tucker, GA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.