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FDA 510(k)

VITAACCESS CATHETER INTRODUCER KIT

K-Number: K890435 · 1989-03-29

ApplicantVitaphore Corp.
Decision Date1989-03-29
Product CodeFOZ
Advisory CommitteeHO
DecisionUnknown

Device Summary

VITAACCESS CATHETER INTRODUCER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Vitaphore Corp.. It received FDA 510(k) clearance on 1989-03-29 under 510(k) number K890435. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the VITAACCESS CATHETER INTRODUCER KIT?

VITAACCESS CATHETER INTRODUCER KIT is a medical device that received FDA 510(k) clearance on 1989-03-29. The listed applicant is Vitaphore Corp.. The 510(k) number is K890435.

When did VITAACCESS CATHETER INTRODUCER KIT receive FDA 510(k) clearance?

VITAACCESS CATHETER INTRODUCER KIT received FDA 510(k) clearance on 1989-03-29, under 510(k) number K890435.

Who is the listed applicant for VITAACCESS CATHETER INTRODUCER KIT?

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

What is the FDA product code for VITAACCESS CATHETER INTRODUCER KIT?

The FDA product code for VITAACCESS CATHETER INTRODUCER KIT is FOZ.

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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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