510(k) K072608

LYOPHILIZED MULTIBLAST MEDIUM KIT by Irvine Scientific Sales Co., Inc. — Product Code MQL

K072608 is an FDA 510(k) premarket notification submitted by Irvine Scientific Sales Co., Inc. for the device "LYOPHILIZED MULTIBLAST MEDIUM KIT". The FDA issued a decision of Substantially Equivalent on Jan 30, 2008. The device falls under product code MQL (Media, Reproductive), a Class II device regulated under 21 CFR 884.6180. Irvine Scientific Sales Co., Inc. has 39 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Jan 30, 2008
Date Received
Sep 17, 2007
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Media, Reproductive
Device Class
Class II
Regulation Number
884.6180
Review Panel
OB
Submission Type
510(k)