510(k) K760073
K760073 is an FDA 510(k) premarket notification submitted by Bemis Health Care for the device "BASIN, WASH, 6-QT RECTANGULAR". The FDA issued a decision of Substantially Equivalent on July 20, 1976. Bemis Health Care has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 20, 1976
- Date Received
- June 18, 1976
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No