510(k) K872524
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 9, 1987
- Date Received
- June 25, 1987
- 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