510(k) K790799
K790799 is an FDA 510(k) premarket notification submitted by Analytic Technology for the device "PULPTESTER MODEL 2001". The FDA issued a decision of Substantially Equivalent on May 31, 1979. The device falls under product code EAT (Tester, Pulp), a Class II device regulated under 21 CFR 872.1720. Analytic Technology has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 31, 1979
- Date Received
- April 24, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Tester, Pulp
- Device Class
- Class II
- Regulation Number
- 872.1720
- Review Panel
- DE
- Submission Type