FDA 510(k)

VISION TRIGLYCERIDES

K-Number: K850031 · 1985-02-04

Decision Date1985-02-04

Product CodeCDT

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

VISION TRIGLYCERIDES is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1985-02-04 under 510(k) number K850031. The device is classified under product code CDT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISION TRIGLYCERIDES?

VISION TRIGLYCERIDES is a medical device that received FDA 510(k) clearance on 1985-02-04. The listed applicant is Abbott Laboratories. The 510(k) number is K850031.

When did VISION TRIGLYCERIDES receive FDA 510(k) clearance?

VISION TRIGLYCERIDES received FDA 510(k) clearance on 1985-02-04, under 510(k) number K850031.

Who is the listed applicant for VISION TRIGLYCERIDES?

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

What is the FDA product code for VISION TRIGLYCERIDES?

The FDA product code for VISION TRIGLYCERIDES is CDT.

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Related Devices (Code: CDT)

K133067ADVIA CHEMISTRY TRIGLYCERIDES_2 (TRIG_2) REAGENTSiemens Healthcare Diagnostics, Inc.K130332VITROS CHEMISTRY PRODUCTS TRIG SLIDESOrtho-Clinical Diagnostics, Inc.K113830VANTERA CLINICAL ANALYZERLiposcience K102993ELITECH CLINICAL SYSTEMS TRIGLYCERIDES SL, ELITECH CLINICAL SYSTEMS CHOLESTEROL SLSeppim S.A.S.K063804OLYMPUS TRIGLYCERIDE TEST SYSTEMOlympus America, Inc.K043546DIMENSION RXL MAX WITH STREAMLAB ANALYTICAL WORKCELL AND SAMPLE TRANSFER MODULEDade Behring, Inc.

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.