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

CUTTER BOND POLYCARBOXYLATE CEMENT

K Number: K821326 · Decision May 28, 1982
Classifications
1
FEI Numbers
144
Registration Numbers
144
Same Product Code
504
Applicant Total
39
Review Days
24

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Basic Information

Device Name
CUTTER BOND POLYCARBOXYLATE CEMENT
K Number
K821326
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3275
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Cutter Laboratories, Inc.
Date Received
May 4, 1982
Decision Date
May 28, 1982
Product Code
EMA
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
EMA Cement, Dental

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Other Clearances by Cutter Laboratories, Inc.

K Number Device Name
K861315 HYPERBARIC PENETRATION EXTENSION SET
K854106 BAYSILEX
K842324 PERFOURM
K834106 INTRAVENOUS INFUSION CONTROLLER
K832237 ORTHOPEDIC CASTING TAPE MAXCAST
K823214 DOSIMETRIC RELEASE PROGRAM - ADMIN. SET
K813532 CUTTERBOND ZINC PHOSPHATE CEMENT
K802105 C-BLADE
K802104 C-SPLINT
K801652 TOTAL PARENTERAL NUTRITION SET BAG
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