510(k) K770368
K770368 is an FDA 510(k) premarket notification submitted by Clairol, Inc. for the device "ORAL IRRIGATOR". The FDA issued a decision of Substantially Equivalent on March 1, 1977. Clairol, Inc. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 1, 1977
- Date Received
- February 23, 1977
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No