510(k) K852999
K852999 is an FDA 510(k) premarket notification submitted by Kallestad Laboratories, Inc. for the device "QVANTIMETRIC 2KAPPA AND LAMBDA TEST KIT". The FDA issued a decision of Substantially Equivalent on October 21, 1985. The device falls under product code DEH (Lambda, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5550. Kallestad Laboratories, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 21, 1985
- Date Received
- July 15, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Lambda, Antigen, Antiserum, Control
- Device Class
- Class II
- Regulation Number
- 866.5550
- Review Panel
- IM
- Submission Type