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

MOBILIMB CPM SHOULDER UNIT

K Number: K891345 · Decision Apr 24, 1989
Classifications
1
FEI Numbers
113
Registration Numbers
113
Same Product Code
159
Applicant Total
11
Review Days
46

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Basic Information

Device Name
MOBILIMB CPM SHOULDER UNIT
K Number
K891345
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.5380
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Toronto Medical Corp.
Date Received
March 9, 1989
Decision Date
April 24, 1989
Product Code
BXB
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
BXB Exerciser, Powered

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (BXB), 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
K900794 MOBILIMB H3 HAND CPM UNIT
K895720 MOBILIMB J1 TMJ CPM UNIT
K880686 TORONTO/MOBILIMB HAND C.P.M.
K880336 MOBILIMB HAND C.P.M. UNIT
Search all 11 clearances from Toronto Medical Corp. →