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FDA 510(k)

FIRST MIDCATH CATHETER

K-Number: K972264 · 1997-09-15

Decision Date1997-09-15
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FIRST MIDCATH CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson Infusion Therapy Systems, Inc.. It received FDA 510(k) clearance on 1997-09-15 under 510(k) number K972264. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIRST MIDCATH CATHETER?

FIRST MIDCATH CATHETER is a medical device that received FDA 510(k) clearance on 1997-09-15. The listed applicant is Becton Dickinson Infusion Therapy Systems, Inc.. The 510(k) number is K972264.

When did FIRST MIDCATH CATHETER receive FDA 510(k) clearance?

FIRST MIDCATH CATHETER received FDA 510(k) clearance on 1997-09-15, under 510(k) number K972264.

Who is the listed applicant for FIRST MIDCATH CATHETER?

The FDA 510(k) record lists Becton Dickinson Infusion Therapy Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FIRST MIDCATH CATHETER?

The FDA product code for FIRST MIDCATH CATHETER is FOZ.

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 Becton Dickinson Infusion Therapy Systems, 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 34 devices →

Related Devices (Code: FOZ)

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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