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

BISCOVER LIQUID POLISH KIT, BISCOVER LIQUID POLISH AND BISCOVER VISCOSITY MODIFIER

K Number: K030354 · Decision Feb 19, 2003
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
50
Applicant Total
79
Review Days
16

Basic Information

Device Name
BISCOVER LIQUID POLISH KIT, BISCOVER LIQUID POLISH AND BISCOVER VISCOSITY MODIFIER
K Number
K030354
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
872.3310
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BISCO, INC.
Date Received
February 3, 2003
Decision Date
February 19, 2003
Product Code
EBD
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
EBD Coating, Filling Material, Resin

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