Olympus Au 5000 Flame Photometer Module

FDA 510(k) K862148 · Olympus Corp.

Substantially Equivalent

510(k) numberK862148

Submission

Device name
Olympus Au 5000 Flame Photometer Module
Applicant
Olympus Corp.
Lake Success, NY, US
Received
June 4, 1986
Decision date
September 29, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

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)DeviceApplicantDecision
K873603Finnigan Mat Incos 50JJO · Traditional Finnigan Corp.09/22/1987SE
K843375Elvi 655 Flame PhotometerJJO · Traditional Logos Scientific, Inc.05/20/1985SE
K841847Lithium ReagentJJO · Traditional Reagent Laboratory, Inc.08/17/1984SE
K834226Flame PhotometersJJO · Traditional Dr. Bruno Lange GmbH06/22/1984SE
K841422Volume Test Dye 6JJO · Traditional Reagent Laboratory, Inc.05/11/1984SE
K841421Daily Wash Solution 5JJO · Traditional Reagent Laboratory, Inc.05/11/1984SE
K840530Supplies for Instrumentation Lab FlameJJO · Traditional Shaban Mfg. Co.03/30/1984SE
K840044Sdi Prepax Dilukit 29-1000JJO · Traditional Scientific Distributors, Inc.03/09/1984SE
K833535Potassium Sodium Analysis ProductsJJO · Traditional Shaban Mfg. Co.12/29/1983SE
K832886Flame Photometer T281-T282-T283JJO · Traditional Texas Intl. Laboratories, Inc.12/08/1983SE

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Questions and answers

When was Olympus Au 5000 Flame Photometer Module cleared by the FDA?

Olympus Au 5000 Flame Photometer Module (K862148) received a 510(k) decision of Substantially Equivalent on September 29, 1986, 117 days after the submission was received.

What is the product code of K862148?

The FDA product code is JJO – Flame Emission Photometer For Clinical Use, a Class I (low risk) device regulated under 21 CFR 862.2540.