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FDA 510(k)

BARD MINI-INFUSER 1500 & 3000

K-Number: K930459 · 1993-08-10

ApplicantBard Medsystems Div.
Decision Date1993-08-10
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BARD MINI-INFUSER 1500 & 3000 is the device name listed in this FDA 510(k) record. The listed applicant is Bard Medsystems Div.. It received FDA 510(k) clearance on 1993-08-10 under 510(k) number K930459. 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 MINI-INFUSER 1500 & 3000?

BARD MINI-INFUSER 1500 & 3000 is a medical device that received FDA 510(k) clearance on 1993-08-10. The listed applicant is Bard Medsystems Div.. The 510(k) number is K930459.

When did BARD MINI-INFUSER 1500 & 3000 receive FDA 510(k) clearance?

BARD MINI-INFUSER 1500 & 3000 received FDA 510(k) clearance on 1993-08-10, under 510(k) number K930459.

Who is the listed applicant for BARD MINI-INFUSER 1500 & 3000?

The FDA 510(k) record lists Bard Medsystems Div. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BARD MINI-INFUSER 1500 & 3000?

The FDA product code for BARD MINI-INFUSER 1500 & 3000 is FRN.

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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.

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