510(k) K934241
K934241 is an FDA 510(k) premarket notification submitted by Advanced Clinical Diagnostics for the device "MCCOY CULTURE CELLS-MCCOY". The FDA issued a decision of Substantially Equivalent on January 3, 1994. The device falls under product code KIR (Cells, Animal And Human, Cultured), a Class I device regulated under 21 CFR 864.2280. Advanced Clinical Diagnostics has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 3, 1994
- Date Received
- August 26, 1993
- 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