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FDA 510(k)

BARD APII PUMP

K-Number: K926385 · 1994-04-18

ApplicantC.R. Bard, Inc.
Decision Date1994-04-18
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BARD APII PUMP 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 1994-04-18 under 510(k) number K926385. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARD APII PUMP?

BARD APII PUMP is a medical device that received FDA 510(k) clearance on 1994-04-18. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K926385.

When did BARD APII PUMP receive FDA 510(k) clearance?

BARD APII PUMP received FDA 510(k) clearance on 1994-04-18, under 510(k) number K926385.

Who is the listed applicant for BARD APII PUMP?

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 APII PUMP?

The FDA product code for BARD APII PUMP is FRN.

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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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