510(k) K781832

SCALE, ACME DIGITAL BEDSIDE by Acme Medical Scale Co. — Product Code FRW

K781832 is an FDA 510(k) premarket notification submitted by Acme Medical Scale Co. for the device "SCALE, ACME DIGITAL BEDSIDE". The FDA issued a decision of Substantially Equivalent on December 7, 1978. 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
December 7, 1978
Date Received
October 30, 1978
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