510(k) K790130
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