FDA 510(k)

BARD NO-RINSE HEMOCONCENTRATOR AND ACCESSORY KIT

K-Number: K971180 · 1997-07-24

Decision Date1997-07-24

Product CodeKDI

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

BARD NO-RINSE HEMOCONCENTRATOR AND ACCESSORY KIT is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1997-07-24 under 510(k) number K971180. The device is classified under product code KDI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD NO-RINSE HEMOCONCENTRATOR AND ACCESSORY KIT?

BARD NO-RINSE HEMOCONCENTRATOR AND ACCESSORY KIT is a medical device that received FDA 510(k) clearance on 1997-07-24. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K971180.

When did BARD NO-RINSE HEMOCONCENTRATOR AND ACCESSORY KIT receive FDA 510(k) clearance?

BARD NO-RINSE HEMOCONCENTRATOR AND ACCESSORY KIT received FDA 510(k) clearance on 1997-07-24, under 510(k) number K971180.

Who is the listed applicant for BARD NO-RINSE HEMOCONCENTRATOR AND ACCESSORY KIT?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BARD NO-RINSE HEMOCONCENTRATOR AND ACCESSORY KIT?

The FDA product code for BARD NO-RINSE HEMOCONCENTRATOR AND ACCESSORY KIT is KDI.

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Official Source

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