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

ARGELITE 52+

K Number: K961211 · Decision Apr 25, 1996
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
626
Applicant Total
217
Review Days
28

Basic Information

Device Name
ARGELITE 52+
K Number
K961211
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3060
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
ARGEN PRECIOUS METALS, INC.
Date Received
March 28, 1996
Decision Date
April 25, 1996
Product Code
EJT
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
EJT Alloy, Gold-Based Noble Metal

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Other Clearances by ARGEN PRECIOUS METALS, INC.

K Number Device Name
K965216 ARGI-SATIN OR OPTI0-STAR
K961352 285 SL
K961285 ARGEDENT 40(GOLD-PALLADIUM-SILVER ALLOY FOR PORCELAIN APPLICATION)
K954362 ARGISTAR 74
K954361 ARGENCO 68M
K954368 ARGEDENT BIO 87 PF
K954371 SUREFIRE S
K954360 ARGESOL 600
K954367 ARGISTAR BIO 75PF
K954358 ARGENDENT GIO 86 FR
Search all 217 clearances from ARGEN PRECIOUS METALS, INC. →