510(k) K861585

ULTRACLONE 01-2300 CELL LINE by Earl-Clay Laboratories, Inc. — Product Code KIR

K861585 is an FDA 510(k) premarket notification submitted by Earl-Clay Laboratories, Inc. for the device "ULTRACLONE 01-2300 CELL LINE". The FDA issued a decision of Substantially Equivalent on May 13, 1986. The device falls under product code KIR (Cells, Animal And Human, Cultured), a Class I device regulated under 21 CFR 864.2280. Earl-Clay Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 13, 1986
Date Received
April 29, 1986
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