510(k) K791348
K791348 is an FDA 510(k) premarket notification submitted by General Clinical Plastics Corp. for the device "ROUND WASHBASIN & RECTANGLE WASHBASIN". The FDA issued a decision of Substantially Equivalent on September 17, 1979. General Clinical Plastics Corp. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 17, 1979
- Date Received
- July 12, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No