510(k) K771434
K771434 is an FDA 510(k) premarket notification submitted by Techhnilab Instruments, Inc. for the device "MULTI-CAVITY EQUILIBRIUM CELL". The FDA issued a decision of Substantially Equivalent on August 22, 1977. Techhnilab Instruments, Inc. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 22, 1977
- Date Received
- August 1, 1977
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No