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FDA 510(k)

SUBCLAVIAN HEMODIALYSIS CATH. W/VITACUFF DEVICE

K-Number: K884325 · 1989-04-25

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1989-04-25
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SUBCLAVIAN HEMODIALYSIS CATH. W/VITACUFF DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1989-04-25 under 510(k) number K884325. 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 SUBCLAVIAN HEMODIALYSIS CATH. W/VITACUFF DEVICE?

SUBCLAVIAN HEMODIALYSIS CATH. W/VITACUFF DEVICE is a medical device that received FDA 510(k) clearance on 1989-04-25. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K884325.

When did SUBCLAVIAN HEMODIALYSIS CATH. W/VITACUFF DEVICE receive FDA 510(k) clearance?

SUBCLAVIAN HEMODIALYSIS CATH. W/VITACUFF DEVICE received FDA 510(k) clearance on 1989-04-25, under 510(k) number K884325.

Who is the listed applicant for SUBCLAVIAN HEMODIALYSIS CATH. W/VITACUFF DEVICE?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUBCLAVIAN HEMODIALYSIS CATH. W/VITACUFF DEVICE?

The FDA product code for SUBCLAVIAN HEMODIALYSIS CATH. W/VITACUFF DEVICE 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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