510(k) K974208
K974208 is an FDA 510(k) premarket notification submitted by Titronics Research & Development Co. for the device "TYTRON C-3000". The FDA issued a decision of Substantially Equivalent on Feb 3, 1998. The device falls under product code HCS (Device, Temperature Measurement, Direct Contact, Powered), a Class II device regulated under 21 CFR 882.1570. Titronics Research & Development Co. has 1 other 510(k) clearance on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 3, 1998
- Date Received
- Nov 10, 1997
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Device, Temperature Measurement, Direct Contact, Powered
- Device Class
- Class II
- Regulation Number
- 882.1570
- Review Panel
- NE
- Submission Type
- 510(k)