Ketosite(Tm)/Stat-Site(Tm)/Ketosite(Tm) Low-Hi Con

FDA 510(k) K911801 · Gds Technology, LLC

Substantially Equivalent

510(k) numberK911801

Submission

Device name
Ketosite(Tm)/Stat-Site(Tm)/Ketosite(Tm) Low-Hi Con
Applicant
Gds Technology, LLC
Elkhart, IN, US
Received
April 23, 1991
Decision date
July 1, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JIN – Nitroprusside, Ketones (Urinary, Non-Quant.)
Device class
Class I (low risk)
Regulation
21 CFR 862.1435
Specialty
Clinical Chemistry

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Questions and answers

When was Ketosite(Tm)/Stat-Site(Tm)/Ketosite(Tm) Low-Hi Con cleared by the FDA?

Ketosite(Tm)/Stat-Site(Tm)/Ketosite(Tm) Low-Hi Con (K911801) received a 510(k) decision of Substantially Equivalent on July 1, 1991, 69 days after the submission was received.

What is the product code of K911801?

The FDA product code is JIN – Nitroprusside, Ketones (Urinary, Non-Quant.), a Class I (low risk) device regulated under 21 CFR 862.1435.