FDA 510(k)

ELVI 165 PROTEO SEROSKOP

K-Number: K842056 · 1984-06-22

Decision Date1984-06-22

Product CodeJQT

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

ELVI 165 PROTEO SEROSKOP is the device name listed in this FDA 510(k) record. The listed applicant is Logos Scientific, Inc.. It received FDA 510(k) clearance on 1984-06-22 under 510(k) number K842056. The device is classified under product code JQT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELVI 165 PROTEO SEROSKOP?

ELVI 165 PROTEO SEROSKOP is a medical device that received FDA 510(k) clearance on 1984-06-22. The listed applicant is Logos Scientific, Inc.. The 510(k) number is K842056.

When did ELVI 165 PROTEO SEROSKOP receive FDA 510(k) clearance?

ELVI 165 PROTEO SEROSKOP received FDA 510(k) clearance on 1984-06-22, under 510(k) number K842056.

Who is the listed applicant for ELVI 165 PROTEO SEROSKOP?

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

What is the FDA product code for ELVI 165 PROTEO SEROSKOP?

The FDA product code for ELVI 165 PROTEO SEROSKOP is JQT.

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Other records listing Logos Scientific, Inc. as applicant

K902614ELVI 828 DIGICLOT MULTISCAN K843375ELVI 655 FLAME PHOTOMETER K844710EUROCHIMA SERUM PROTEIN ELECTROPHORESIS METHOD K843296ELVI 675 DIGITRON K842313ELVI 146 SEROSCAN K841804ELVI 70 SAFETY CHAMBER

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Related Devices (Code: JQT)

K111356ASIMANAGER - ATArlington Scientific, Inc.K944185ISOSCANIsolab, Inc.K915332MODEL 795 FLUOROMETER/DENSITOMETERCiba Corning Diagnostics Corp.K885254TARGET READERV-Tech, Inc.K860645ELECTROPHORESIS DATA CENTER (EDC)Helena Laboratories K862956ICON READERHybritech, 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.