510(k) K822124
K822124 is an FDA 510(k) premarket notification submitted by Helena Laboratories for the device "TITAN GEL CPK ISOENZYME SYSTEM". The FDA issued a decision of Substantially Equivalent on November 1, 1982. The device falls under product code JHT (Chromatographic Separation, Cpk Isoenzymes), a Class II device regulated under 21 CFR 862.1215. Helena Laboratories has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 1, 1982
- Date Received
- July 19, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Chromatographic Separation, Cpk Isoenzymes
- Device Class
- Class II
- Regulation Number
- 862.1215
- Review Panel
- CH
- Submission Type