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FDA 510(k)

IQ POTASSIUM

K-Number: K881440 · 1988-05-27

Decision Date1988-05-27
Product CodeCEJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IQ POTASSIUM 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 1988-05-27 under 510(k) number K881440. The device is classified under product code CEJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IQ POTASSIUM?

IQ POTASSIUM is a medical device that received FDA 510(k) clearance on 1988-05-27. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K881440.

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

IQ POTASSIUM received FDA 510(k) clearance on 1988-05-27, under 510(k) number K881440.

Who is the listed applicant for IQ POTASSIUM?

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 POTASSIUM?

The FDA product code for IQ POTASSIUM is CEJ.

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 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.

View all 632 devices →

Related Devices (Code: CEJ)

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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