FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

E 4000 DENTAL OPERATING CHAIR

K Number: K925567 · Decision Mar 10, 1994
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
62
Applicant Total
13
Review Days
492

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Basic Information

Device Name
E 4000 DENTAL OPERATING CHAIR
K Number
K925567
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.6250
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Dentalez Group
Date Received
November 3, 1992
Decision Date
March 10, 1994
Product Code
KLC
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
KLC Chair, Dental, With Operative Unit

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K983574 STARDENTAL TITAN 3 LUBEFREE MOTOR ATTACHMENTS
K982593 LUBE FREE AUTOCHUCK TURBINE WITH VORTEX AIR SEAL FOR USE WITH STAR DENTAL 430 SERIES LUBE FREE HIGH SPEED DENTAL HANDPIE
K960719 STAR DENTAL 430 SERIES HIGH SPEED HANDPIECE
K960507 STAR DENTAL PUSHBUTTON AUTOCHUCK REPLACEMENT TURBINE FOR MIDWEST HANDPIECES
K960260 STAR TITAN SERIES MOTORS & ATTACHMENTS
K931093 QUICK-CONNECT 360 SWIVEL TIP AUTOCLAVABLE SYRINGE
K902402 HIGH SPEED NON-FIBER OPTIC SWIVEL HANDPIECE
Search all 13 clearances from Dentalez Group →