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FDA 510(k)

3M CDI H/S CUVETTES WITH HEPARON TREATMENT

K-Number: K973472 · 1997-12-08

Applicant3M Healthcare
Decision Date1997-12-08
Product CodeDRY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

3M CDI H/S CUVETTES WITH HEPARON TREATMENT is the device name listed in this FDA 510(k) record. The listed applicant is 3M Healthcare. It received FDA 510(k) clearance on 1997-12-08 under 510(k) number K973472. 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 3M CDI H/S CUVETTES WITH HEPARON TREATMENT?

3M CDI H/S CUVETTES WITH HEPARON TREATMENT is a medical device that received FDA 510(k) clearance on 1997-12-08. The listed applicant is 3M Healthcare. The 510(k) number is K973472.

When did 3M CDI H/S CUVETTES WITH HEPARON TREATMENT receive FDA 510(k) clearance?

3M CDI H/S CUVETTES WITH HEPARON TREATMENT received FDA 510(k) clearance on 1997-12-08, under 510(k) number K973472.

Who is the listed applicant for 3M CDI H/S CUVETTES WITH HEPARON TREATMENT?

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

What is the FDA product code for 3M CDI H/S CUVETTES WITH HEPARON TREATMENT?

The FDA product code for 3M CDI H/S CUVETTES WITH HEPARON TREATMENT is 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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