Blood GASES/PC02, PO2 Analysis Products

FDA 510(k) K902267 · Phoenix Diagnostics, Inc.

Substantially Equivalent

510(k) numberK902267

Submission

Device name
Blood GASES/PC02, PO2 Analysis Products
Applicant
Phoenix Diagnostics, Inc.
Medfield, MA, US
Received
May 21, 1990
Decision date
June 12, 1990
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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Questions and answers

When was Blood GASES/PC02, PO2 Analysis Products cleared by the FDA?

Blood GASES/PC02, PO2 Analysis Products (K902267) received a 510(k) decision of Substantially Equivalent on June 12, 1990, 22 days after the submission was received.

What is the product code of K902267?

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.