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

HAND INSTRUMENTS

K Number: K760985 · Decision Nov 15, 1976
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
6
Applicant Total
11
Review Days
25

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Basic Information

Device Name
HAND INSTRUMENTS
K Number
K760985
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4565
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Adp Intl., Inc.
Date Received
October 21, 1976
Decision Date
November 15, 1976
Product Code
EKW
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
EKW Broach, Endodontic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EKW), ordered by most recent decision date.

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Other Clearances by Adp Intl., Inc.

K Number Device Name
K760988 DENTAL HANDPIECES
K760983 ENDODONTIC INSTRUMENTS
K760980 DENTAL ALLOY
K760984 ORTHODONTIC INSTRUMENTS
K760982 DENTAL VARNISH
K760979 COMPOSITE MATERIAL
K760987 DIAMOND STONES
K760986 CARBIDE DENTAL BURS
K760978 ZINC CEMENT
K760981 ALGINATE IMPRESSION MATERIAL
Search all 11 clearances from Adp Intl., Inc. →