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

POIRIER POWERED WHEELCHAIR

K Number: K864791 · Decision Feb 4, 1987
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
580
Applicant Total
24
Review Days
58

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Basic Information

Device Name
POIRIER POWERED WHEELCHAIR
K Number
K864791
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
890.3860
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Roseburg SA
Date Received
December 8, 1986
Decision Date
February 4, 1987
Product Code
ITI
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
ITI Wheelchair, Powered

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K882392 BURNET LABORATOIRE PHARMACEUTIQUE SURGICAL GLOVES
K872715 UNIVERSAL INSTRUMENTATION(CD) FOR SPINAL SURGERY
K874317 POIRIER KID-ROLLER MANUAL WHEELCHAIR
K872714 S.T.A.C.E.M. EXTERNAL BREAST PROSTHESIS MAMMARY
K871688 SPECTACLE FRAME - DANIELLE
K871689 SPECTACLE FRAME - LORRAINE
K870654 EFER ARTHROSCOPE
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