510(k) K930261
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