Continuous Single Culture Complete

FDA 510(k) K121572 · Irvine Scientific Sales Co., Inc.

Substantially Equivalent

510(k) numberK121572

Submission

Device name
Continuous Single Culture Complete
Applicant
Irvine Scientific Sales Co., Inc.
Santa Ana, CA, US
Received
May 29, 2012
Decision date
July 19, 2012
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MQL – Media, Reproductive
Device class
Class II (moderate risk)
Regulation
21 CFR 884.6180
Specialty
Obstetrics/Gynecology

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K121128Multipurpose Handling MediumMQL · Traditional 06/06/2012SE
K093273Vit Kit - Freeze and ThawMQL · Traditional 03/03/2010SE
K072609Single Step MediumMQL · Traditional 02/12/2008SE
K072608Lyophilized Multiblast Medium KitMQL · Traditional 01/30/2008SE
K072607Lyophilized Early Cleavage Medium (Ecm) KitMQL · Traditional 01/25/2008SE
K061549Amniostat-Flm-PgJHG · Traditional 10/18/2006SE
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Questions and answers

When was Continuous Single Culture Complete cleared by the FDA?

Continuous Single Culture Complete (K121572) received a 510(k) decision of Substantially Equivalent on July 19, 2012, 51 days after the submission was received.

What is the product code of K121572?

The FDA product code is MQL – Media, Reproductive, a Class II (moderate risk) device regulated under 21 CFR 884.6180.