FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

INTERJET(TM) GINGIVAL CARE INSTRUMENT

K Number: K921999 · Decision Jun 3, 1992
Classifications
1
FEI Numbers
213
Registration Numbers
214
Same Product Code
46
Applicant Total
92
Review Days
35

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Basic Information

Device Name
INTERJET(TM) GINGIVAL CARE INSTRUMENT
K Number
K921999
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6510
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bausch & Lomb, Inc.
Date Received
April 29, 1992
Decision Date
June 3, 1992
Product Code
EFS
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EFS Unit, Oral Irrigation

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K113852 BAUSCH & LOMB IOL INJECTOR
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K111877 EZS05 CLEANING AND DISINFECTING SOLUTION, BAUSCH + LOMB EZS05 CLEANING AND DISINFECTING SOLUTION
K112192 NATURELLE DAILY DISPOSABLE (HILAFILCON B) COSMETICALLY TINTED CONTACT LENS
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