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FDA 510(k)

SODIUM & POTASSIUM PRODUCTS

K-Number: K813127 · 1982-01-22

Decision Date1982-01-22
Product CodeJIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SODIUM & POTASSIUM PRODUCTS is the device name listed in this FDA 510(k) record. The listed applicant is Alko Diagnostic Corp.. It received FDA 510(k) clearance on 1982-01-22 under 510(k) number K813127. The device is classified under product code JIX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SODIUM & POTASSIUM PRODUCTS?

SODIUM & POTASSIUM PRODUCTS is a medical device that received FDA 510(k) clearance on 1982-01-22. The listed applicant is Alko Diagnostic Corp.. The 510(k) number is K813127.

When did SODIUM & POTASSIUM PRODUCTS receive FDA 510(k) clearance?

SODIUM & POTASSIUM PRODUCTS received FDA 510(k) clearance on 1982-01-22, under 510(k) number K813127.

Who is the listed applicant for SODIUM & POTASSIUM PRODUCTS?

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

What is the FDA product code for SODIUM & POTASSIUM PRODUCTS?

The FDA product code for SODIUM & POTASSIUM PRODUCTS is JIX.

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 Alko Diagnostic Corp. 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 31 devices →

Related Devices (Code: JIX)

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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