510(k) K781832
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