510(k) K830171

DIGITAL BEDSIDE SCALE #5000 by Acme Medical Scale Co. — Product Code FRW

K830171 is an FDA 510(k) premarket notification submitted by Acme Medical Scale Co. for the device "DIGITAL BEDSIDE SCALE #5000". The FDA issued a decision of Substantially Equivalent on February 18, 1983. The device falls under product code FRW (Scale, Patient), a Class I device regulated under 21 CFR 880.2720. Acme Medical Scale Co. has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 18, 1983
Date Received
January 18, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Scale, Patient
Device Class
Class I
Regulation Number
880.2720
Review Panel
HO
Submission Type