510(k) K893602

GLASS MERCURY FILLED THERMOMETERS by Smith & Nephew United, Inc. — Product Code FLK

K893602 is an FDA 510(k) premarket notification submitted by Smith & Nephew United, Inc. for the device "GLASS MERCURY FILLED THERMOMETERS". The FDA issued a decision of Substantially Equivalent on August 8, 1989. The device falls under product code FLK (Thermometer, Clinical Mercury), a Class II device regulated under 21 CFR 880.2920. Smith & Nephew United, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 8, 1989
Date Received
May 15, 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