510(k) K832696
K832696 is an FDA 510(k) premarket notification submitted by Imex Medical Systems, Inc. for the device "RISER STANDUP WHEELCHAIR". The FDA issued a decision of Substantially Equivalent on September 20, 1983. The device falls under product code IPL (Wheelchair, Standup), a Class II device regulated under 21 CFR 890.3900. Imex Medical Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 20, 1983
- Date Received
- August 10, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Wheelchair, Standup
- Device Class
- Class II
- Regulation Number
- 890.3900
- Review Panel
- PM
- Submission Type