Ciba Corning Model 280 Ph/Blood Gas System

FDA 510(k) K880353 · Ciba Corning Diagnostics Corp.

Substantially Equivalent

510(k) numberK880353

Submission

Device name
Ciba Corning Model 280 Ph/Blood Gas System
Applicant
Ciba Corning Diagnostics Corp.
East Walpole, MA, US
Received
January 26, 1988
Decision date
June 15, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GKR – System, Hemoglobin, Automated
Device class
Class II (moderate risk)
Regulation
21 CFR 864.5620
Specialty
Hematology

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Questions and answers

When was Ciba Corning Model 280 Ph/Blood Gas System cleared by the FDA?

Ciba Corning Model 280 Ph/Blood Gas System (K880353) received a 510(k) decision of Substantially Equivalent on June 15, 1988, 141 days after the submission was received.

What is the product code of K880353?

The FDA product code is GKR – System, Hemoglobin, Automated, a Class II (moderate risk) device regulated under 21 CFR 864.5620.