510(k) K880069
K880069 is an FDA 510(k) premarket notification submitted by Leeco Diagnostics, Inc. for the device "LEECO PREGNASTICK (EIA) CATALOG #003". The FDA issued a decision of Substantially Equivalent on February 11, 1988. The device falls under product code LCX (Kit, Test, Pregnancy, Hcg, Over The Counter), a Class II device regulated under 21 CFR 862.1155. Leeco Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 11, 1988
- Date Received
- January 11, 1988
- 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