510(k) K962306

FRESH CELLS MULTI-WELL & SHELL VIAL CULTURES by Diagnostic Hybrids, Inc. — Product Code KIR

K962306 is an FDA 510(k) premarket notification submitted by Diagnostic Hybrids, Inc. for the device "FRESH CELLS MULTI-WELL & SHELL VIAL CULTURES". The FDA issued a decision of Substantially Equivalent on August 29, 1996. 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
August 29, 1996
Date Received
June 17, 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