510(k) K893602
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