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

PARAPOST SYSTEM STERILIZABLE ORGANIZER

K Number: K993835 · Decision Dec 16, 1999
Classifications
1
FEI Numbers
194
Registration Numbers
194
Same Product Code
321
Applicant Total
21
Review Days
34

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Basic Information

Device Name
PARAPOST SYSTEM STERILIZABLE ORGANIZER
K Number
K993835
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Coltene/Whaledent, Inc.
Date Received
November 12, 1999
Decision Date
December 16, 1999
Product Code
FRG
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
FRG Wrap, Sterilization

Similar 510(k) Clearances

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Other Clearances by Coltene/Whaledent, Inc.

K Number Device Name
K071632 PERFECT TISSUE CONTOURING SYSTEM II
K051660 DENTRONIX DDS 7000 RAPID DRY HEAT STERILIZER STERILIZATION SYSTEM
K040551 COLTOLUX LED CURING LIGHT
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
Search all 21 clearances from Coltene/Whaledent, Inc. →