FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

LIGHT-CURE

K Number: K952858 · Decision Sep 5, 1995
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
192
Applicant Total
7
Review Days
75

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Basic Information

Device Name
LIGHT-CURE
K Number
K952858
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3750
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Midwest Orthodontic Mfg.
Date Received
June 22, 1995
Decision Date
September 5, 1995
Product Code
DYH
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
DYH Adhesive, Bracket And Tooth Conditioner, Resin

Similar 510(k) Clearances

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

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Other Clearances by Midwest Orthodontic Mfg.

K Number Device Name
K981433 ORTHODONTIC BRACES
K955740 GLUFLORMA
K952856 LIGHT-CURE PC
K952855 PC-LOCK
K952857 PRO-LOCK
K900824 FLUOR-I-CHAINS(TM) AND FLUOR-I-TIES(TM)