510(k) K811703
K811703 is an FDA 510(k) premarket notification submitted by William Harvey Life Products Corp. for the device "CARDIFF ALDASORBER SYSTEM". The FDA issued a decision of SESP on Jun 16, 1981. William Harvey Life Products Corp. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESP ()
- Decision Date
- Jun 16, 1981
- Date Received
- Jun 16, 1981
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No