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FDA 510(k)

BARD HARVARD MINI-INFUSER 400 MULTI DOSE SYRINGE

K-Number: K844730 · 1985-01-28

Decision Date1985-01-28
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BARD HARVARD MINI-INFUSER 400 MULTI DOSE SYRINGE 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 1985-01-28 under 510(k) number K844730. 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 HARVARD MINI-INFUSER 400 MULTI DOSE SYRINGE?

BARD HARVARD MINI-INFUSER 400 MULTI DOSE SYRINGE is a medical device that received FDA 510(k) clearance on 1985-01-28. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K844730.

When did BARD HARVARD MINI-INFUSER 400 MULTI DOSE SYRINGE receive FDA 510(k) clearance?

BARD HARVARD MINI-INFUSER 400 MULTI DOSE SYRINGE received FDA 510(k) clearance on 1985-01-28, under 510(k) number K844730.

Who is the listed applicant for BARD HARVARD MINI-INFUSER 400 MULTI DOSE SYRINGE?

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 HARVARD MINI-INFUSER 400 MULTI DOSE SYRINGE?

The FDA product code for BARD HARVARD MINI-INFUSER 400 MULTI DOSE SYRINGE 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.

View all 616 devices →

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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