510(k) K841350
K841350 is an FDA 510(k) premarket notification submitted by E. Benson Hood Laboratories, Inc. for the device "SALIVARY BYPASS TUBE". The FDA issued a decision of Substantially Equivalent on July 26, 1984. E. Benson Hood Laboratories, Inc. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 26, 1984
- Date Received
- April 2, 1984
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No