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

DENTRONIX DDS 7000 RAPID DRY HEAT STERILIZER STERILIZATION SYSTEM

K Number: K051660 · Decision Aug 4, 2005
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
9
Applicant Total
21
Review Days
43

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Basic Information

Device Name
DENTRONIX DDS 7000 RAPID DRY HEAT STERILIZER STERILIZATION SYSTEM
K Number
K051660
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6870
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Coltene/Whaledent, Inc.
Date Received
June 22, 2005
Decision Date
August 4, 2005
Product Code
KMH
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KMH Sterilizer, Dry Heat

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Other Clearances by Coltene/Whaledent, Inc.

K Number Device Name
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K033760 ONE COAT SE BOND
K031752 COLTOSOL F
K013400 SYNERGY FLOW
K003034 COLTENE AURA COMPOMER RESTORATIVE SYSTEM
K993545 TENAX WHITE POST
K000311 PARAPOST FIBER WHITE
K993710 MODIFICATION OF PARAPOST CEMENT
K993835 PARAPOST SYSTEM STERILIZABLE ORGANIZER
Search all 21 clearances from Coltene/Whaledent, Inc. →