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

PERMA-CRYL 20

K Number: K792427 · Decision Dec 13, 1979
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
329
Applicant Total
20
Review Days
16

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Basic Information

Device Name
PERMA-CRYL 20
K Number
K792427
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3760
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Coe Laboratories, Inc.
Date Received
November 27, 1979
Decision Date
December 13, 1979
Product Code
EBI
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
EBI Resin, Denture, Relining, Repairing, Rebasing

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Other Clearances by Coe Laboratories, Inc.

K Number Device Name
K903292 ACCUFLEX/ACCUMIX VINYL POLY IMPRESSION MATERIALS
K894282 FIRST IMPRESSION TM
K894281 FIRST IMPRESSION WITH CHLORHEXIDINE
K891140 OCCLU-SEAL(TM) VISIBLE LIGHT-CURED FISSURE SEALANT
K885010 TRIPTON(TM) VISIBLE LIGHT-CURED UNIV. BONDING
K881422 COE PAK AUTO MIX, REGULAR OR HARD SET
K881091 OMNISIL, VINYL POLYSILOXANE IMPRESSION MATERIAL
K863882 OPALUX VISIBLE LIGHT CURED ANTERIOR COMPOSITE
K842877 ABSOLUTE VINYL POLYSILOXANE IMPRESS
K844325 COE-LITE POLYMERIZATION UNIT
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