510(k) K973212

FRESH CELLS WI-38 by Diagnostic Hybrids, Inc. — Product Code KIR

K973212 is an FDA 510(k) premarket notification submitted by Diagnostic Hybrids, Inc. for the device "FRESH CELLS WI-38". The FDA issued a decision of Substantially Equivalent on September 25, 1997. The device falls under product code KIR (Cells, Animal And Human, Cultured), a Class I device regulated under 21 CFR 864.2280. Diagnostic Hybrids, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 25, 1997
Date Received
August 27, 1997
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