510(k) K930261

RTM REHABILITATION TREADMILL, MODEL #945-200 by Biodan Medical Systems, Ltd. — Product Code IOL

K930261 is an FDA 510(k) premarket notification submitted by Biodan Medical Systems, Ltd. for the device "RTM REHABILITATION TREADMILL, MODEL #945-200". The FDA issued a decision of Substantially Equivalent on May 26, 1993. The device falls under product code IOL (Treadmill, Powered), a Class I device regulated under 21 CFR 890.5380. Biodan Medical Systems, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 26, 1993
Date Received
January 19, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Treadmill, Powered
Device Class
Class I
Regulation Number
890.5380
Review Panel
PM
Submission Type