510(k) K871319
K871319 is an FDA 510(k) premarket notification submitted by Helena Laboratories for the device "TITAN GEL MULTI-SLOT LIPO-17 SYSTEM". The FDA issued a decision of Substantially Equivalent on April 22, 1987. 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
- April 22, 1987
- Date Received
- April 3, 1987
- 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