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FDA 510(k)

CDI 100 EXTRACORPOREAL HEMATOCRIT/OXYGEN SATURATIO

K-Number: K931968 · 1993-11-10

Applicant3M Health Care, Ltd.
Decision Date1993-11-10
Product CodeDRY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CDI 100 EXTRACORPOREAL HEMATOCRIT/OXYGEN SATURATIO is the device name listed in this FDA 510(k) record. The listed applicant is 3M Health Care, Ltd.. It received FDA 510(k) clearance on 1993-11-10 under 510(k) number K931968. The device is classified under product code DRY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CDI 100 EXTRACORPOREAL HEMATOCRIT/OXYGEN SATURATIO?

CDI 100 EXTRACORPOREAL HEMATOCRIT/OXYGEN SATURATIO is a medical device that received FDA 510(k) clearance on 1993-11-10. The listed applicant is 3M Health Care, Ltd.. The 510(k) number is K931968.

When did CDI 100 EXTRACORPOREAL HEMATOCRIT/OXYGEN SATURATIO receive FDA 510(k) clearance?

CDI 100 EXTRACORPOREAL HEMATOCRIT/OXYGEN SATURATIO received FDA 510(k) clearance on 1993-11-10, under 510(k) number K931968.

Who is the listed applicant for CDI 100 EXTRACORPOREAL HEMATOCRIT/OXYGEN SATURATIO?

The FDA 510(k) record lists 3M Health Care, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CDI 100 EXTRACORPOREAL HEMATOCRIT/OXYGEN SATURATIO?

The FDA product code for CDI 100 EXTRACORPOREAL HEMATOCRIT/OXYGEN SATURATIO is DRY.

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Related Devices (Code: DRY)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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