Acid Base System, Radiometer Automated

FDA 510(k) K760229 · The London Co.

Substantially Equivalent

510(k) numberK760229

Submission

Device name
Acid Base System, Radiometer Automated
Applicant
The London Co.
Mchenry, IL, US
Received
July 14, 1976
Decision date
August 26, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CHL – Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1120
Specialty
Clinical Chemistry

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More from Opti Medical Systems, Inc.

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K802846TCM202 TCPO2 & TCM204 TCPO2/PO2 Rec. Sy.KLK · Traditional 12/17/1980SE
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K780652Hemoglobin Check Solutions, S2100 OSM-2JKS · Traditional 07/27/1978SE
K771444Qualicheck TMJJS · Traditional 08/16/1977SE
K771263Radiomhter OSM-2 HemoximeterGHS · Traditional 08/03/1977SE

Questions and answers

When was Acid Base System, Radiometer Automated cleared by the FDA?

Acid Base System, Radiometer Automated (K760229) received a 510(k) decision of Substantially Equivalent on August 26, 1976, 43 days after the submission was received.

What is the product code of K760229?

The FDA product code is CHL – Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph, a Class II (moderate risk) device regulated under 21 CFR 862.1120.