Reagents for Astra 8 Automated Analyzer

FDA 510(k) K801222 · Simmler, Inc.

Substantially Equivalent

510(k) numberK801222

Submission

Device name
Reagents for Astra 8 Automated Analyzer
Applicant
Simmler, Inc.
Mchenry, IL, US
Received
May 23, 1980
Decision date
June 26, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JIX – Calibrator, Multi-Analyte Mixture
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1150
Specialty
Clinical Chemistry

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K123321Dimension Chemistry III CalibratoryJIX · Traditional Siemens Healthcare Diagnostics02/15/2013SE
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More from Siemens Healthcare Diagnostics, Inc.

510(k)DeviceDecision
K895745Sickle Cell Solubility Test KitJBB · Traditional 11/29/1989SE
K874903Multichem(R) Y -Glutamyltransferase (Y -Gt)JPZ · Traditional 02/11/1988SE
K874595Multichem (R) Magnesium ReagentJGJ · Traditional 01/21/1988SE
K874820Multichem HDL Precipitating Reagent #S0914LBR · Traditional 01/07/1988SE
K874812Multichem Chloride Reagent S0933CHJ · Traditional 12/18/1987SE
K874311Multichem (R) Total BilirubinCIG · Traditional 11/25/1987SE
K874049Multichem Albumin Reagent S0902CIX · Traditional 10/29/1987SE
K874038Multichem Inorganic Phosphorous S0923CEO · Traditional 10/28/1987SE
K873725Multichem Creatinine Reagent S0917CGX · Traditional 10/20/1987SE
K873761Multichem Alkaline Phosphatase (S0903)CJE · Traditional 10/07/1987SE

Questions and answers

When was Reagents for Astra 8 Automated Analyzer cleared by the FDA?

Reagents for Astra 8 Automated Analyzer (K801222) received a 510(k) decision of Substantially Equivalent on June 26, 1980, 34 days after the submission was received.

What is the product code of K801222?

The FDA product code is JIX – Calibrator, Multi-Analyte Mixture, a Class II (moderate risk) device regulated under 21 CFR 862.1150.