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

QUINTON MEDTRACK CR PLUS TREADMILL

K Number: K990866 · Decision Apr 29, 1999
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
60
Applicant Total
164
Review Days
44

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Basic Information

Device Name
QUINTON MEDTRACK CR PLUS TREADMILL
K Number
K990866
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.5360
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Quinton, Inc.
Date Received
March 16, 1999
Decision Date
April 29, 1999
Product Code
ISD
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
ISD Exerciser, Measuring

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K001492 QUINTON Q-STRESS, MODEL 000483
K992908 Q-TEL TELEMETRY SYSTEM V. 6.0 (ST)
K971397 VIEWCATH 3-D CATHETER PULLBACK
K964784 SYNERGY CARDIOLOGY INFORMATION SYSTEM (00431)
K964978 VITAL STATISTICS SYSTEM (O-CATH ACCESSORY)
K955002 MAHURKAR 8 FR DUAL LEMEN CATHETER
K961014 QUINTON MODEL Q710 EXERCISE AND RESTING ELECTROCARDIOGRAPH
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