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FDA 510(k)

BARD 500ML RESERVOIR HOLDER

K-Number: K915649 · 1994-03-07

Decision Date1994-03-07
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BARD 500ML RESERVOIR HOLDER 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 1994-03-07 under 510(k) number K915649. 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 500ML RESERVOIR HOLDER?

BARD 500ML RESERVOIR HOLDER is a medical device that received FDA 510(k) clearance on 1994-03-07. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K915649.

When did BARD 500ML RESERVOIR HOLDER receive FDA 510(k) clearance?

BARD 500ML RESERVOIR HOLDER received FDA 510(k) clearance on 1994-03-07, under 510(k) number K915649.

Who is the listed applicant for BARD 500ML RESERVOIR HOLDER?

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 500ML RESERVOIR HOLDER?

The FDA product code for BARD 500ML RESERVOIR HOLDER is FRN.

Related Clinical Trials

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.

Other records listing C.R. Bard, Inc. as applicant

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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Related Devices (Code: FRN)

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.

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.

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