Microflame Photometer
FDA 510(k) K792087 · Gilford Instrument Laboratories, Inc.
510(k) numberK792087
Submission
- Device name
- Microflame Photometer
- Applicant
- Gilford Instrument Laboratories, Inc.
Mchenry, IL, US - Received
- October 17, 1979
- Decision date
- November 13, 1979
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- JJO – Flame Emission Photometer For Clinical Use
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 862.2540
- Specialty
- Clinical Chemistry
Other 510(k)s with product code JJO
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K873603 | Finnigan Mat Incos 50JJO · Traditional | Finnigan Corp. | 09/22/1987SE |
| K862148 | Olympus Au 5000 Flame Photometer ModuleJJO · Traditional | Olympus Corp. | 09/29/1986SE |
| K843375 | Elvi 655 Flame PhotometerJJO · Traditional | Logos Scientific, Inc. | 05/20/1985SE |
| K841847 | Lithium ReagentJJO · Traditional | Reagent Laboratory, Inc. | 08/17/1984SE |
| K834226 | Flame PhotometersJJO · Traditional | Dr. Bruno Lange GmbH | 06/22/1984SE |
| K841422 | Volume Test Dye 6JJO · Traditional | Reagent Laboratory, Inc. | 05/11/1984SE |
| K841421 | Daily Wash Solution 5JJO · Traditional | Reagent Laboratory, Inc. | 05/11/1984SE |
| K840530 | Supplies for Instrumentation Lab FlameJJO · Traditional | Shaban Mfg. Co. | 03/30/1984SE |
| K840044 | Sdi Prepax Dilukit 29-1000JJO · Traditional | Scientific Distributors, Inc. | 03/09/1984SE |
| K833535 | Potassium Sodium Analysis ProductsJJO · Traditional | Shaban Mfg. Co. | 12/29/1983SE |
More from Shaban Mfg. Co.
| 510(k) | Device | Decision |
|---|---|---|
| K823233 | Sba 300 Clinical Chemistry AnalyzerJJC · Traditional | 11/29/1982SE |
| K821583 | Ames/Gilford Optimate Clin. Chem & TherJJF · Traditional | 06/24/1982SE |
| K802609 | Chemistry Analyzer Impact 400JJE · Traditional | 11/26/1980SE |
| K801889 | Model 203S Clinical Chemistry AnalyzerJJE · Traditional | 09/26/1980SE |
| K800085 | System 203 Chemistry AnalyzerJJE · Traditional | 02/13/1980SE |
| K792361 | System 103 Chemistry AnalyzerJJE · Traditional | 12/27/1979SE |
| K791968 | Eia (Elisa) ReaderJJQ · Traditional | 10/17/1979SE |
| K790073 | Analyzer, Impact 100JJI · Traditional | 02/22/1979SE |
| K790072 | Analyzer, Impact 200JJE · Traditional | 02/22/1979SE |
| K781269 | Elisa SystmeJJQ · Traditional | 12/04/1978SE |
Questions and answers
When was Microflame Photometer cleared by the FDA?
Microflame Photometer (K792087) received a 510(k) decision of Substantially Equivalent on November 13, 1979, 27 days after the submission was received.
What is the product code of K792087?
The FDA product code is JJO – Flame Emission Photometer For Clinical Use, a Class I (low risk) device regulated under 21 CFR 862.2540.