510(k) K934245

HUMAN FORESKIN FIBROBLAST CELLS-H.F.F. by Advanced Clinical Diagnostics — Product Code KIR

K934245 is an FDA 510(k) premarket notification submitted by Advanced Clinical Diagnostics for the device "HUMAN FORESKIN FIBROBLAST CELLS-H.F.F.". 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