Finnigan Mat Incos 50

FDA 510(k) K873603 · Finnigan Corp.

Substantially Equivalent

510(k) numberK873603

Submission

Device name
Finnigan Mat Incos 50
Applicant
Finnigan Corp.
San Jose, CA, US
Received
September 4, 1987
Decision date
September 22, 1987
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
K862148Olympus Au 5000 Flame Photometer ModuleJJO · Traditional Olympus Corp.09/29/1986SE
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

More from Texas Intl. Laboratories, Inc.

510(k)DeviceDecision
K880418Incos 50 Mass SpectrometerDOP · Traditional 05/31/1988SE
K880090Ion Trap DetectorDOP · Traditional 03/15/1988SE
K880089Finnigan Mat TSQ-70DOP · Traditional 02/11/1988SE

Questions and answers

When was Finnigan Mat Incos 50 cleared by the FDA?

Finnigan Mat Incos 50 (K873603) received a 510(k) decision of Substantially Equivalent on September 22, 1987, 18 days after the submission was received.

What is the product code of K873603?

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