510(k) K922024
K922024 is an FDA 510(k) premarket notification submitted by Helena Laboratories for the device "REP SPE PLUS (ACID BLUE) SYSTEM,# 3173/3174/3175". The FDA issued a decision of Substantially Equivalent on July 23, 1992. The device falls under product code CEF (Electrophoretic, Protein Fractionation), a Class I device regulated under 21 CFR 862.1630. Helena Laboratories has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 23, 1992
- Date Received
- May 1, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Electrophoretic, Protein Fractionation
- Device Class
- Class I
- Regulation Number
- 862.1630
- Review Panel
- CH
- Submission Type