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FDA 510(k)

3M CDI QUICK-CELLS WITH HEPARIN TREATMENT

K-Number: K980732 · 1998-05-15

Applicant3M Healthcare
Decision Date1998-05-15
Product CodeDRY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

3M CDI QUICK-CELLS WITH HEPARIN 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 1998-05-15 under 510(k) number K980732. 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 QUICK-CELLS WITH HEPARIN TREATMENT?

3M CDI QUICK-CELLS WITH HEPARIN TREATMENT is a medical device that received FDA 510(k) clearance on 1998-05-15. The listed applicant is 3M Healthcare. The 510(k) number is K980732.

When did 3M CDI QUICK-CELLS WITH HEPARIN TREATMENT receive FDA 510(k) clearance?

3M CDI QUICK-CELLS WITH HEPARIN TREATMENT received FDA 510(k) clearance on 1998-05-15, under 510(k) number K980732.

Who is the listed applicant for 3M CDI QUICK-CELLS WITH HEPARIN 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 QUICK-CELLS WITH HEPARIN TREATMENT?

The FDA product code for 3M CDI QUICK-CELLS WITH HEPARIN TREATMENT 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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