510(k) K790130
K790130 is an FDA 510(k) premarket notification submitted by Acme Medical Scale Co. for the device "SCALE, DIGITAL CHAIR". The FDA issued a decision of Substantially Equivalent on February 1, 1979. The device falls under product code FRI (Scale, Stand-On, Patient), a Class I device regulated under 21 CFR 880.2700. Acme Medical Scale Co. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 1, 1979
- Date Received
- January 23, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Scale, Stand-On, Patient
- Device Class
- Class I
- Regulation Number
- 880.2700
- Review Panel
- HO
- Submission Type