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

51-210 TO 51-352 VARIOUS INTEST FOR CALLIS, LOCKWO

K Number: K851796 · Decision Jun 20, 1985
Classifications
1
FEI Numbers
455
Registration Numbers
456
Same Product Code
103
Applicant Total
79
Review Days
56

Basic Information

Device Name
51-210 TO 51-352 VARIOUS INTEST FOR CALLIS, LOCKWO
K Number
K851796
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
ARTIBERIA
Date Received
April 25, 1985
Decision Date
June 20, 1985
Product Code
GEN
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GEN Forceps, General & Plastic Surgery

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K851723 1300/10 TO 1305/89-92 VARIOUS CUTTING INSTRUMENTS
K851719 1070/15 TO 1078/17 VARIOUS TYPES NEEDLE HOLDERS
K851724 1410/1 TO 1435/13 VARIOUS PROBES & EXPLORERS
K851726 1760/1 TO 2010/34 VARIOUS DENTAL FILLING INSTRUMEN
K851730 2710 TO 2935 VARIOUS PLIERS FOR ORTHODONTICS/PROST
K851729 2620/1 TO 2635/2 VARIOUS DENTAL CROWN SCISSORS
K851722 1285/5 TO 1295 VARIOUS TYPES OF DENTAL EXCAVATORS
K851727 2020-1/2 TO 2220 VARIOUS DENTAL WAX & MODELLING CA
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