Serim Disintek Gta 2.1%, Model: 5164

FDA 510(k) K083295 · Serim Research Corp.

Substantially Equivalent

510(k) numberK083295

Submission

Device name
Serim Disintek Gta 2.1%, Model: 5164
Applicant
Serim Research Corp.
Elkhart, IN, US
Received
November 10, 2008
Decision date
March 16, 2009
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JOJ – Indicator, Physical/Chemical Sterilization Process
Device class
Class II (moderate risk)
Regulation
21 CFR 880.2800
Specialty
General Hospital

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Questions and answers

When was Serim Disintek Gta 2.1%, Model: 5164 cleared by the FDA?

Serim Disintek Gta 2.1%, Model: 5164 (K083295) received a 510(k) decision of Substantially Equivalent on March 16, 2009, 126 days after the submission was received.

What is the product code of K083295?

The FDA product code is JOJ – Indicator, Physical/Chemical Sterilization Process, a Class II (moderate risk) device regulated under 21 CFR 880.2800.