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

STATUSBLUE

K Number: K013237 · Decision Oct 22, 2001
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
401
Applicant Total
28
Review Days
24

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Basic Information

Device Name
STATUSBLUE
K Number
K013237
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
872.3660
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dmg USA, Inc.
Date Received
September 28, 2001
Decision Date
October 22, 2001
Product Code
ELW
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
ELW Material, Impression

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Other Clearances by Dmg USA, Inc.

K Number Device Name
K171772 Ecosite Bulk Fill
K160443 TempoCem Clear
K130580 RETRACTION PASTE
K110759 TEMPOCEM
K102603 SA FLOWABLE ADHESIVE
K101710 LUXATEMP ULTRA /STAR
K100062 INFILTRATION KIT
K093338 SELF ADHESIVE COMPOSITE LUTING CEMENT
K093587 DENTAL MERCURY
K081493 INFILTRATION KIT
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