510(k) K924441

U.S. MEDICAL PS-6000 WHEELCHAIR SCALE by U.S. Medical Corp. — Product Code INF

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