510(k) K936171

TRANSFORMED PRIMARY HUMAN EMBRYONAL KIDNEY by Advanced Clinical Diagnostics — Product Code KIR

K936171 is an FDA 510(k) premarket notification submitted by Advanced Clinical Diagnostics for the device "TRANSFORMED PRIMARY HUMAN EMBRYONAL KIDNEY". The FDA issued a decision of Substantially Equivalent on February 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
February 3, 1994
Date Received
December 23, 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