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FDA 510(k)

ELVI 18

K-Number: K841288 · 1984-05-02

ApplicantLogos Scientific, Inc.
Decision Date1984-05-02
Product CodeJJN
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ELVI 18 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 1984-05-02 under 510(k) number K841288. The device is classified under product code JJN. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELVI 18?

ELVI 18 is a medical device that received FDA 510(k) clearance on 1984-05-02. The listed applicant is Logos Scientific, Inc.. The 510(k) number is K841288.

When did ELVI 18 receive FDA 510(k) clearance?

ELVI 18 received FDA 510(k) clearance on 1984-05-02, under 510(k) number K841288.

Who is the listed applicant for ELVI 18?

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 18?

The FDA product code for ELVI 18 is JJN.

Other records listing Logos Scientific, 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.

K902614ELVI 828 DIGICLOT MULTISCANK843375ELVI 655 FLAME PHOTOMETERK844710EUROCHIMA SERUM PROTEIN ELECTROPHORESIS METHODK843296ELVI 675 DIGITRONK842313ELVI 146 SEROSCANK842056ELVI 165 PROTEO SEROSKOP

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Related Devices (Code: JJN)

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.

K924021POWER SUPPLYThe Binding Site, Ltd.K924020ELECTROPHORESIS TANKThe Binding Site, Ltd.K882344ELECTR-TRANSBLOTTERThe W.E.P. Co.K881852REP SP ELECTROPHORESIS SYSTEM CAT NO. 3170Helena LaboratoriesK882163HELENA REP GEL PROCESSORHelena LaboratoriesK873352RAPID ELECTROPHORESIS SYSTEM (REP)Helena Laboratories

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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