510(k) K880686

TORONTO/MOBILIMB HAND C.P.M. by Toronto Medical Corp. — Product Code JFA

K880686 is an FDA 510(k) premarket notification submitted by Toronto Medical Corp. for the device "TORONTO/MOBILIMB HAND C.P.M.". The FDA issued a decision of Substantially Equivalent on February 26, 1988. The device falls under product code JFA (Exerciser, Finger, Powered), a Class I device regulated under 21 CFR 890.5410. Toronto Medical Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 26, 1988
Date Received
February 19, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Exerciser, Finger, Powered
Device Class
Class I
Regulation Number
890.5410
Review Panel
PM
Submission Type