510(k) K924441
K924441 is an FDA 510(k) premarket notification submitted by U.S. Medical Corp. for the device "U.S. MEDICAL PS-6000 WHEELCHAIR SCALE". The FDA issued a decision of Substantially Equivalent on February 12, 1993. The device falls under product code INF (Scale, Platform, Wheelchair), a Class I device regulated under 21 CFR 890.3940. U.S. Medical Corp. has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 12, 1993
- Date Received
- September 1, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Scale, Platform, Wheelchair
- Device Class
- Class I
- Regulation Number
- 890.3940
- Review Panel
- PM
- Submission Type