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

STERILE WATER SYSTEM

K Number: K823230 · Decision Dec 3, 1982
Classifications
1
FEI Numbers
111
Registration Numbers
111
Same Product Code
283
Applicant Total
3
Review Days
35

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Basic Information

Device Name
STERILE WATER SYSTEM
K Number
K823230
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6640
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Syntex Dental Products, Inc.
Date Received
October 29, 1982
Decision Date
December 3, 1982
Product Code
EIA
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
EIA Unit, Operative Dental

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Other Clearances by Syntex Dental Products, Inc.

K Number Device Name
K832378 VIBRATORY ENDODONTIC SYSTEM
K822610 PRECAPSULED DENTAL AMALGAM