510(k) K960909
K960909 is an FDA 510(k) premarket notification submitted by Neogenex for the device "H292 CELL CULTURE". The FDA issued a decision of Substantially Equivalent on May 30, 1996. The device falls under product code KIR (Cells, Animal And Human, Cultured), a Class I device regulated under 21 CFR 864.2280. Neogenex has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 30, 1996
- Date Received
- March 5, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Cells, Animal And Human, Cultured
- Device Class
- Class I
- Regulation Number
- 864.2280
- Review Panel
- PA
- Submission Type