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FDA 510(k)

REFEREE AQUEOUS TRIGLYCERIDE STND

K-Number: K760806 · 1976-10-21

Decision Date1976-10-21
Product CodeJIS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

REFEREE AQUEOUS TRIGLYCERIDE STND is the device name listed in this FDA 510(k) record. The listed applicant is Analytical Products, Inc.. It received FDA 510(k) clearance on 1976-10-21 under 510(k) number K760806. The device is classified under product code JIS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REFEREE AQUEOUS TRIGLYCERIDE STND?

REFEREE AQUEOUS TRIGLYCERIDE STND is a medical device that received FDA 510(k) clearance on 1976-10-21. The listed applicant is Analytical Products, Inc.. The 510(k) number is K760806.

When did REFEREE AQUEOUS TRIGLYCERIDE STND receive FDA 510(k) clearance?

REFEREE AQUEOUS TRIGLYCERIDE STND received FDA 510(k) clearance on 1976-10-21, under 510(k) number K760806.

Who is the listed applicant for REFEREE AQUEOUS TRIGLYCERIDE STND?

The FDA 510(k) record lists Analytical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REFEREE AQUEOUS TRIGLYCERIDE STND?

The FDA product code for REFEREE AQUEOUS TRIGLYCERIDE STND is JIS.

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 Analytical Products, Inc. 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 57 devices →

Related Devices (Code: JIS)

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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