510(k) K894772
K894772 is an FDA 510(k) premarket notification submitted by Medtech Instruments for the device "THERMALGRAPHIC ANALYSER". The FDA issued a decision of Substantially Equivalent on Oct 3, 1989. The device falls under product code HCS (Device, Temperature Measurement, Direct Contact, Powered), a Class II device regulated under 21 CFR 882.1570. Medtech Instruments has 1 other 510(k) clearance on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 3, 1989
- Date Received
- Jul 26, 1989
- 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)