510(k) K013466
K013466 is an FDA 510(k) premarket notification submitted by Helena Laboratories for the device "SPIFE 2000/3000 LIPOPROTEIN; MODEL# 3340, 3341, 3342, 3343". The FDA issued a decision of Substantially Equivalent on December 21, 2001. The device falls under product code JHO (Electrophoretic Separation, Lipoproteins), a Class I device regulated under 21 CFR 862.1475. Helena Laboratories has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 21, 2001
- Date Received
- October 18, 2001
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Electrophoretic Separation, Lipoproteins
- Device Class
- Class I
- Regulation Number
- 862.1475
- Review Panel
- CH
- Submission Type