510(k) K880686
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