510(k) K022330
K022330 is an FDA 510(k) premarket notification submitted by <Genx> Intl., Inc. for the device "ALLGRAD 45 AND 90 CELL SEPARATION MEDIA". The FDA issued a decision of Substantially Equivalent on August 26, 2002. The device falls under product code MQL (Media, Reproductive), a Class II device regulated under 21 CFR 884.6180. <Genx> Intl., Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 26, 2002
- Date Received
- July 18, 2002
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Media, Reproductive
- Device Class
- Class II
- Regulation Number
- 884.6180
- Review Panel
- OB
- Submission Type