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FDA 510(k)

CYBREX TM FPQ FLUORESCENE POLARIZATION

K-Number: K802579 · 1980-11-12

ApplicantAbbott Laboratories
Decision Date1980-11-12
Product CodeKHO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CYBREX TM FPQ FLUORESCENE POLARIZATION is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K802579. The device is classified under product code KHO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CYBREX TM FPQ FLUORESCENE POLARIZATION?

CYBREX TM FPQ FLUORESCENE POLARIZATION is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Abbott Laboratories. The 510(k) number is K802579.

When did CYBREX TM FPQ FLUORESCENE POLARIZATION receive FDA 510(k) clearance?

CYBREX TM FPQ FLUORESCENE POLARIZATION received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802579.

Who is the listed applicant for CYBREX TM FPQ FLUORESCENE POLARIZATION?

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 CYBREX TM FPQ FLUORESCENE POLARIZATION?

The FDA product code for CYBREX TM FPQ FLUORESCENE POLARIZATION is KHO.

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Related Devices (Code: KHO)

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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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