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FDA 510(k)

FLOW-PAC CHLORIDE REAGENT SET

K-Number: K834333 · 1984-02-21

Decision Date1984-02-21
Product CodeCHJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FLOW-PAC CHLORIDE REAGENT SET is the device name listed in this FDA 510(k) record. The listed applicant is American Research Products Co.. It received FDA 510(k) clearance on 1984-02-21 under 510(k) number K834333. The device is classified under product code CHJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOW-PAC CHLORIDE REAGENT SET?

FLOW-PAC CHLORIDE REAGENT SET is a medical device that received FDA 510(k) clearance on 1984-02-21. The listed applicant is American Research Products Co.. The 510(k) number is K834333.

When did FLOW-PAC CHLORIDE REAGENT SET receive FDA 510(k) clearance?

FLOW-PAC CHLORIDE REAGENT SET received FDA 510(k) clearance on 1984-02-21, under 510(k) number K834333.

Who is the listed applicant for FLOW-PAC CHLORIDE REAGENT SET?

The FDA 510(k) record lists American Research Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLOW-PAC CHLORIDE REAGENT SET?

The FDA product code for FLOW-PAC CHLORIDE REAGENT SET is CHJ.

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 American Research Products Co. 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 56 devices →

Related Devices (Code: CHJ)

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

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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