510(k) K840412
K840412 is an FDA 510(k) premarket notification submitted by Monoclonal Antibodies, Inc. for the device "OVU STICK URINE HLH KIT". The FDA issued a decision of Substantially Equivalent on April 13, 1984. The device falls under product code CEP (Radioimmunoassay, Luteinizing Hormone), a Class I device regulated under 21 CFR 862.1485. Monoclonal Antibodies, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 13, 1984
- Date Received
- January 31, 1984
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Radioimmunoassay, Luteinizing Hormone
- Device Class
- Class I
- Regulation Number
- 862.1485
- Review Panel
- CH
- Submission Type