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FDA 510(k)

AUTOMATED EIA MICROPLATE READER MODELS EL340/340I

K-Number: K901059 · 1990-04-09

Decision Date1990-04-09
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AUTOMATED EIA MICROPLATE READER MODELS EL340/340I is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Tek Instruments, Inc.. It received FDA 510(k) clearance on 1990-04-09 under 510(k) number K901059. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOMATED EIA MICROPLATE READER MODELS EL340/340I?

AUTOMATED EIA MICROPLATE READER MODELS EL340/340I is a medical device that received FDA 510(k) clearance on 1990-04-09. The listed applicant is Bio-Tek Instruments, Inc.. The 510(k) number is K901059.

When did AUTOMATED EIA MICROPLATE READER MODELS EL340/340I receive FDA 510(k) clearance?

AUTOMATED EIA MICROPLATE READER MODELS EL340/340I received FDA 510(k) clearance on 1990-04-09, under 510(k) number K901059.

Who is the listed applicant for AUTOMATED EIA MICROPLATE READER MODELS EL340/340I?

The FDA 510(k) record lists Bio-Tek Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTOMATED EIA MICROPLATE READER MODELS EL340/340I?

The FDA product code for AUTOMATED EIA MICROPLATE READER MODELS EL340/340I is JJQ.

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 Bio-Tek Instruments, 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.

View all 37 devices →

Related Devices (Code: JJQ)

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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