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

IVORY PREMIUM RUBBER DAM

K Number: K863816 · Decision Oct 27, 1986
Classifications
1
FEI Numbers
110
Registration Numbers
110
Same Product Code
32
Applicant Total
11
Review Days
27

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Basic Information

Device Name
IVORY PREMIUM RUBBER DAM
K Number
K863816
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6300
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Columbus Dental Mfg. Co.
Date Received
September 30, 1986
Decision Date
October 27, 1986
Product Code
EIE
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
EIE Dam, Rubber

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K872243 PEKALUX(TM)
K872272 PEKALUX/GLUMA LIGHT CURED ANTERIOR RESTORATIVE SYS
K871164 GLUMA(TM) BONDING SYSTEM
K871165 LUMIFOR(TM) COMPOSITE
K863758 ORTHO-BITE WAX WAFER
K860855 SHUR GEL 4
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