510(k) K940852
K940852 is an FDA 510(k) premarket notification submitted by Redman, Inc. for the device "CHIEF STANDUP WHEELCHAIR". The FDA issued a decision of SN on Feb 3, 1995. The device falls under product code IPL (Wheelchair, Standup), a Class II device regulated under 21 CFR 890.3900. Redman, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SN ()
- Decision Date
- Feb 3, 1995
- Date Received
- Feb 23, 1994
- 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