510(k) K770501
K770501 is an FDA 510(k) premarket notification submitted by Robert R. Moore for the device "KNEE CUFF FOR EXPRESSING FLUID". The FDA issued a decision of Substantially Equivalent on April 5, 1977. Robert R. Moore has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 5, 1977
- Date Received
- March 15, 1977
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No