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FDA 510(k)

ALFERR TIBC TUBE

K-Number: K864548 · 1987-02-02

ApplicantBenchmark Reagents
Decision Date1987-02-02
Product CodeJQE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ALFERR TIBC TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Benchmark Reagents. It received FDA 510(k) clearance on 1987-02-02 under 510(k) number K864548. The device is classified under product code JQE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALFERR TIBC TUBE?

ALFERR TIBC TUBE is a medical device that received FDA 510(k) clearance on 1987-02-02. The listed applicant is Benchmark Reagents. The 510(k) number is K864548.

When did ALFERR TIBC TUBE receive FDA 510(k) clearance?

ALFERR TIBC TUBE received FDA 510(k) clearance on 1987-02-02, under 510(k) number K864548.

Who is the listed applicant for ALFERR TIBC TUBE?

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

What is the FDA product code for ALFERR TIBC TUBE?

The FDA product code for ALFERR TIBC TUBE is JQE.

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Related Devices (Code: JQE)

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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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