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

RX APF (CASTING ALLOY)

K Number: K890811 · Decision Mar 17, 1989
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
193
Applicant Total
78
Review Days
29

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Basic Information

Device Name
RX APF (CASTING ALLOY)
K Number
K890811
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3060
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Jeneric/Pentron, Inc.
Date Received
February 16, 1989
Decision Date
March 17, 1989
Product Code
EJS
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
EJS Alloy, Other Noble Metal

Similar 510(k) Clearances

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

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Other Clearances by Jeneric/Pentron, Inc.

K Number Device Name
K020499 BOND-3 ADHESIVE
K013543 BOND-1 C & B
K013542 DENTIN CONDITIONING AND ADHESIVE SYSTEM (BOND-1)
K012231 AVANTE MICRO CRYSTAL SYSTEM
K011748 FIRST FILL R.C.S.
K010957 QUELL DESENSITIZER
K011330 JP CAST 50
K011331 JP CAST 40
K011362 GOLD CORE 73 LS
K010044 COSMIC
Search all 78 clearances from Jeneric/Pentron, Inc. →