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

QUICKIE TSR

K Number: K952641 · Decision Jul 6, 1995
Classifications
1
FEI Numbers
123
Registration Numbers
123
Same Product Code
445
Applicant Total
19
Review Days
27

Basic Information

Device Name
QUICKIE TSR
K Number
K952641
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
SUNRISE MEDICAL, INC.
Date Received
June 9, 1995
Decision Date
July 6, 1995
Product Code
IOR
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
IOR Wheelchair, Mechanical

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Other Clearances by SUNRISE MEDICAL, INC.

K Number Device Name
K072153 QUICKIE QX MANUAL FOLDING WHEELCHAIR
K062701 QUICKIE RHAPSODY, MWD SERIES II POWER WHEELCHAIR
K031289 QUICKIE FREESTYLE POWER WHEELCHAIR, MODEL G-424
K010917 POWER TILT AND RECLINE SYSTEM
K011268 BREEZY WHEELCHAIR, MODEL 300
K001491 QUICKIE 2 POWER ASSIST WHEELCHAIR
K981885 SUNRISE SCOOTER SERIES, MODEL UNASSIGNED, 3 WHEEL STANDARD MODEL, 3 WHEEL MID RANGE MODEL, 3 WHEEL HIGH END MODEL, 4 WHE
K983677 QUICKIE G SERIES, MODEL G-424
K981462 QUICKIE P100 SERIES, QUICKIE P200 SERIES, QUICKIE P300 SERIES, MODELS P100,P110,P120,P190,P190R,P500,P200,P210,P320,P300
K983520 BREATH CONTROL (BREATH ACTUATOR), SENSITOUCH BREATH CONTROL, HEAD ARRAY (SWITCH HEAD CONTROL), TRI-SWITCH HEAD ARRAY, HD
Search all 19 clearances from SUNRISE MEDICAL, INC. →