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FDA 510(k)

SARNS MEMBRANE OXGENATOR PART NUMBER 9443

K-Number: K903436 · 1990-10-19

Applicant3M Health Care, Sarns
Decision Date1990-10-19
Product CodeDTZ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SARNS MEMBRANE OXGENATOR PART NUMBER 9443 is the device name listed in this FDA 510(k) record. The listed applicant is 3M Health Care, Sarns. It received FDA 510(k) clearance on 1990-10-19 under 510(k) number K903436. The device is classified under product code DTZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SARNS MEMBRANE OXGENATOR PART NUMBER 9443?

SARNS MEMBRANE OXGENATOR PART NUMBER 9443 is a medical device that received FDA 510(k) clearance on 1990-10-19. The listed applicant is 3M Health Care, Sarns. The 510(k) number is K903436.

When did SARNS MEMBRANE OXGENATOR PART NUMBER 9443 receive FDA 510(k) clearance?

SARNS MEMBRANE OXGENATOR PART NUMBER 9443 received FDA 510(k) clearance on 1990-10-19, under 510(k) number K903436.

Who is the listed applicant for SARNS MEMBRANE OXGENATOR PART NUMBER 9443?

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

What is the FDA product code for SARNS MEMBRANE OXGENATOR PART NUMBER 9443?

The FDA product code for SARNS MEMBRANE OXGENATOR PART NUMBER 9443 is DTZ.

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Other records listing 3M Health Care, Sarns as applicant

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Related Devices (Code: DTZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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