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

BISTITE II SC

K Number: K991711 · Decision Jul 7, 1999
Classifications
1
FEI Numbers
144
Registration Numbers
144
Same Product Code
504
Applicant Total
22
Review Days
49

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Basic Information

Device Name
BISTITE II SC
K Number
K991711
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3275
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tokuyama America, Inc.
Date Received
May 19, 1999
Decision Date
July 7, 1999
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 Tokuyama America, Inc.

K Number Device Name
K022641 TOKUYAMA REBASE II
K011854 TOKUYAMA M-BOND
K011685 BISTITE II DC
K010267 PALFIQUE ESTELITE LV CLEAR
K002863 PALFIQUE ESTELITE LV
K993917 TOKUYAMA ONE-UP-BOND F
K982537 TOKUYAMA SOFRELINER
K980054 PALFIQUE ESTELITE
K980058 TOKUSO MAC BOND II
K980051 PALFIQUE ESTELITE PASTE
Search all 22 clearances from Tokuyama America, Inc. →