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

CUTTER SIL-SILICONE IMPRESSION MAT

K Number: K760755 · Decision Oct 15, 1976
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
401
Applicant Total
39
Review Days
14

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Basic Information

Device Name
CUTTER SIL-SILICONE IMPRESSION MAT
K Number
K760755
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3660
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Cutter Laboratories, Inc.
Date Received
October 1, 1976
Decision Date
October 15, 1976
Product Code
ELW
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
ELW Material, Impression

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K834106 INTRAVENOUS INFUSION CONTROLLER
K832237 ORTHOPEDIC CASTING TAPE MAXCAST
K823214 DOSIMETRIC RELEASE PROGRAM - ADMIN. SET
K821326 CUTTER BOND POLYCARBOXYLATE CEMENT
K813532 CUTTERBOND ZINC PHOSPHATE CEMENT
K802105 C-BLADE
K802104 C-SPLINT
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