FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

RESTORE-PF VIC; RESTORE-PF VLC CAPSULE

K Number: K011295 · Decision Jun 27, 2001
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
5
Review Days
58

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Basic Information

Device Name
RESTORE-PF VIC; RESTORE-PF VLC CAPSULE
K Number
K011295
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
First Scientific Limited
Date Received
April 30, 2001
Decision Date
June 27, 2001
Product Code
EBF
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
EBF Material, Tooth Shade, Resin

Similar 510(k) Clearances

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

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Other Clearances by First Scientific Limited

K Number Device Name
K011521 ORTHO VLC; ORTHO VLC CAPSULE
K011520 RESTORE-X
K011517 LUTE; CORE
K011309 LUTE VLC; CORE VLC