Synermed Serum IRON-600 Reagent Kit
FDA 510(k) K912912 · Synermed, Inc.
510(k) numberK912912
Submission
- Device name
- Synermed Serum IRON-600 Reagent Kit
- Applicant
- Synermed, Inc.
Quebec, Canada, CA - Received
- July 3, 1991
- Decision date
- July 30, 1991
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
Device classification
- Product code
- CFM – Bathophenanthroline, Colorimetry, Iron (Non-Heme)
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 862.1410
- Specialty
- Clinical Chemistry
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|---|---|---|---|
| K984119 | Wako L-Type Fe, Wako L-Type CalibratorCFM · Traditional | Wako Chemicals USA, Inc. | 01/15/1999SE |
| K981581 | IronCFM · Traditional | Abbott Laboratories | 06/08/1998SE |
| K932871 | Uibc for Discreet Random Access AnalyzerCFM · Traditional | Catachem, Inc. | 09/08/1993SE |
| K913705 | Abbott Qluickstart Iron Test, Item #5A29CFM · Traditional | Em Diagnostic Systems, Inc. | 10/09/1991SE |
| K902918 | Synermed Serum Iron Reagent KitCFM · Traditional | Synermed, Inc. | 07/31/1990SE |
| K895047 | Clinistat Potassium Reagent TestCFM · Traditional | Heraeus Kulzer, Inc. | 10/17/1989SE |
| K891155 | Iron ReagentCFM · Traditional | Medical Analysis Systems, Inc. | 04/18/1989SE |
| K873120 | Abbott A-Gent Iron Reagent KitCFM · Traditional | Abbott Laboratories | 08/25/1987SE |
| K861602 | Total Iron Binding Capacity ProcedureCFM · Traditional | Data Medical Associates, Inc. | 05/23/1986SE |
| K854305 | Dart Iron & Iron Binding Capacity ReagentCFM · Traditional | Coulter Electronics, Inc. | 11/12/1985SE |
More from Coulter Electronics, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K973109 | Synermed Near-Infrared Direct Bilirubin Reagent KitCIG · Traditional | 09/25/1997SE |
| K972716 | Synermed Total Bilirubin Reagent KitCIG · Traditional | 08/07/1997SE |
| K971491 | Synermed Ir 200 Chemistry AnalyzerJJF · Traditional | 06/26/1997SE |
| K962479 | Synermed Ise ReagentsCGZ · Traditional | 03/03/1997SE |
| K963939 | Synermed Direct Bilirubin Reagent KitCIG · Traditional | 12/18/1996SE |
| K960793 | Synermed Enzymatic CO2 Reagent KitKHS · Traditional | 03/11/1996SE |
| K953395 | Synermed Calcium Reagent KitCJY · Traditional | 08/31/1995SE |
| K952179 | Synermed Ise ReagentsJGS · Traditional | 06/20/1995SE |
| K943924 | Creatinine-Po Reagent KitCGX · Traditional | 09/20/1994SE |
| K941091 | Synermed Amylase Reagent KitJFJ · Traditional | 05/03/1994SE |
Questions and answers
When was Synermed Serum IRON-600 Reagent Kit cleared by the FDA?
Synermed Serum IRON-600 Reagent Kit (K912912) received a 510(k) decision of Substantially Equivalent on July 30, 1991, 27 days after the submission was received.
What is the product code of K912912?
The FDA product code is CFM – Bathophenanthroline, Colorimetry, Iron (Non-Heme), a Class I (low risk) device regulated under 21 CFR 862.1410.