510(k) K897054
K897054 is an FDA 510(k) premarket notification submitted by Cypress Medical Products, Ltd. for the device "CLINICAL MERCURY THERMOMETER". The FDA issued a decision of Substantially Equivalent on March 22, 1990. The device falls under product code FLK (Thermometer, Clinical Mercury), a Class II device regulated under 21 CFR 880.2920. Cypress Medical Products, Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 22, 1990
- Date Received
- December 18, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Thermometer, Clinical Mercury
- Device Class
- Class II
- Regulation Number
- 880.2920
- Review Panel
- HO
- Submission Type