Uropaper Eiken AG

FDA 510(k) K843757 · Syn-Kit, Inc.

Substantially Equivalent

510(k) numberK843757

Submission

Device name
Uropaper Eiken AG
Applicant
Syn-Kit, Inc.
Mchenry, IL, US
Received
September 25, 1984
Decision date
December 18, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JIL – Method, Enzymatic, Glucose (Urinary, Non-Quantitative)
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1340
Specialty
Clinical Chemistry

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More from Teco Diagnostics

510(k)DeviceDecision
K861098Seroiden Strepto Kit 'Eiken'GTZ · Traditional 08/12/1986SE
K861631Slide Culture U 'Eiken'JXA · Traditional 06/10/1986SE
K854819CPR Slide EikenDCN · Traditional 02/26/1986SE
K854820Ra 80 EikenDHR · Traditional 01/17/1986SE
K853276Aso Slide EikenGTQ · Traditional 08/20/1985SE
K843760Uropaper Eiken GJIL · Traditional 12/18/1984SE
K843759Uropaper Eiken HagJIL · Traditional 12/18/1984SE
K843758Uropaper Eiken GKJIL · Traditional 12/18/1984SE
K843756Uropaper Eiken 5JIL · Traditional 12/18/1984SE
K843755Uropaper Eiken 6BJIL · Traditional 12/18/1984SE

Questions and answers

When was Uropaper Eiken AG cleared by the FDA?

Uropaper Eiken AG (K843757) received a 510(k) decision of Substantially Equivalent on December 18, 1984, 84 days after the submission was received.

What is the product code of K843757?

The FDA product code is JIL – Method, Enzymatic, Glucose (Urinary, Non-Quantitative), a Class II (moderate risk) device regulated under 21 CFR 862.1340.