510(k) K200913
K200913 is an FDA 510(k) premarket notification submitted by Spd Swiss Precision Diagnostics GmbH for the device "Clearblue® Early Digital Pregnancy Test". The FDA issued a decision of Substantially Equivalent on August 13, 2021. The device falls under product code LCX (Kit, Test, Pregnancy, Hcg, Over The Counter), a Class II device regulated under 21 CFR 862.1155. Spd Swiss Precision Diagnostics GmbH has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 13, 2021
- Date Received
- April 6, 2020
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Kit, Test, Pregnancy, Hcg, Over The Counter
- Device Class
- Class II
- Regulation Number
- 862.1155
- Review Panel
- CH
- Submission Type