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FDA 510(k)

IQ ALKALINE PHOSPHATASE

K-Number: K880344 · 1988-03-01

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1988-03-01
Product CodeCJK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IQ ALKALINE PHOSPHATASE 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 1988-03-01 under 510(k) number K880344. The device is classified under product code CJK. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IQ ALKALINE PHOSPHATASE?

IQ ALKALINE PHOSPHATASE is a medical device that received FDA 510(k) clearance on 1988-03-01. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K880344.

When did IQ ALKALINE PHOSPHATASE receive FDA 510(k) clearance?

IQ ALKALINE PHOSPHATASE received FDA 510(k) clearance on 1988-03-01, under 510(k) number K880344.

Who is the listed applicant for IQ ALKALINE PHOSPHATASE?

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 ALKALINE PHOSPHATASE?

The FDA product code for IQ ALKALINE PHOSPHATASE is CJK.

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Other records listing Bd Becton Dickinson Vacutainer Systems Preanalytic 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.

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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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