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

MOBILIMB H3 HAND CPM UNIT

K Number: K900794 · Decision Mar 2, 1990
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
11
Applicant Total
11
Review Days
10

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Basic Information

Device Name
MOBILIMB H3 HAND CPM UNIT
K Number
K900794
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.5410
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Toronto Medical Corp.
Date Received
February 20, 1990
Decision Date
March 2, 1990
Product Code
JFA
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
JFA Exerciser, Finger, Powered

Similar 510(k) Clearances

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

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Other Clearances by Toronto Medical Corp.

K Number Device Name
K950682 W2 WRIST CPM UNIT
K935587 MULTILINK SHOULDER CPM UNIT
K935841 DR KOOL
K925926 MOBILIMB T1 TOE CPM UNIT
K900466 MOBILIMB W1 WRIST CPM UNIT
K900795 MOBILIMB L4 LOWER LIMB CPM UNIT
K895720 MOBILIMB J1 TMJ CPM UNIT
K891345 MOBILIMB CPM SHOULDER UNIT
K880686 TORONTO/MOBILIMB HAND C.P.M.
K880336 MOBILIMB HAND C.P.M. UNIT
Search all 11 clearances from Toronto Medical Corp. →