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FDA 510(k)

OLYMPUS IGG IMMUNOTURBIDIMETRIC REAGENT

K-Number: K951013 · 1995-04-17

Decision Date1995-04-17
Product CodeCFQ
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

OLYMPUS IGG IMMUNOTURBIDIMETRIC REAGENT is the device name listed in this FDA 510(k) record. The listed applicant is Olympus America, Inc.. It received FDA 510(k) clearance on 1995-04-17 under 510(k) number K951013. The device is classified under product code CFQ. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS IGG IMMUNOTURBIDIMETRIC REAGENT?

OLYMPUS IGG IMMUNOTURBIDIMETRIC REAGENT is a medical device that received FDA 510(k) clearance on 1995-04-17. The listed applicant is Olympus America, Inc.. The 510(k) number is K951013.

When did OLYMPUS IGG IMMUNOTURBIDIMETRIC REAGENT receive FDA 510(k) clearance?

OLYMPUS IGG IMMUNOTURBIDIMETRIC REAGENT received FDA 510(k) clearance on 1995-04-17, under 510(k) number K951013.

Who is the listed applicant for OLYMPUS IGG IMMUNOTURBIDIMETRIC REAGENT?

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

What is the FDA product code for OLYMPUS IGG IMMUNOTURBIDIMETRIC REAGENT?

The FDA product code for OLYMPUS IGG IMMUNOTURBIDIMETRIC REAGENT is CFQ.

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 Olympus America, 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.

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Related Devices (Code: CFQ)

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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