510(k) K897054

CLINICAL MERCURY THERMOMETER by Cypress Medical Products, Ltd. — Product Code FLK

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