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FDA 510(k)

IQ ALBUMIN

K-Number: K891375 · 1989-05-05

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1989-05-05
Product CodeCIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IQ ALBUMIN 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 1989-05-05 under 510(k) number K891375. The device is classified under product code CIX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IQ ALBUMIN?

IQ ALBUMIN is a medical device that received FDA 510(k) clearance on 1989-05-05. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K891375.

When did IQ ALBUMIN receive FDA 510(k) clearance?

IQ ALBUMIN received FDA 510(k) clearance on 1989-05-05, under 510(k) number K891375.

Who is the listed applicant for IQ ALBUMIN?

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 IQ ALBUMIN?

The FDA product code for IQ ALBUMIN is CIX.

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Other records listing Bd Becton Dickinson Vacutainer Systems Preanalytic as applicant

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Related Devices (Code: CIX)

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.

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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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