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FDA 510(k)

FLOW-PAC SHOLESTEROL REAGENT SET

K-Number: K832780 · 1983-10-14

Decision Date1983-10-14
Product CodeCHH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FLOW-PAC SHOLESTEROL 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 1983-10-14 under 510(k) number K832780. The device is classified under product code CHH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOW-PAC SHOLESTEROL REAGENT SET?

FLOW-PAC SHOLESTEROL REAGENT SET is a medical device that received FDA 510(k) clearance on 1983-10-14. The listed applicant is American Research Products Co.. The 510(k) number is K832780.

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

FLOW-PAC SHOLESTEROL REAGENT SET received FDA 510(k) clearance on 1983-10-14, under 510(k) number K832780.

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

The FDA product code for FLOW-PAC SHOLESTEROL REAGENT SET is CHH.

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: CHH)

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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