FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇦 Canada

PERSONAL BACK WITH FIP KIT

K Number: K894770 · Decision Sep 11, 1989
Classifications
1
FEI Numbers
137
Registration Numbers
137
Same Product Code
63
Applicant Total
2
Review Days
47

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Basic Information

Device Name
PERSONAL BACK WITH FIP KIT
K Number
K894770
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3920
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Canadian Posture and Seating Centre, Inc.
Date Received
July 26, 1989
Decision Date
September 11, 1989
Product Code
KNN
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
KNN Components, Wheelchair

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KNN), ordered by most recent decision date.

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Other Clearances by Canadian Posture and Seating Centre, Inc.

K Number Device Name
K894767 CORNER SEAT