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FDA 510(k)

AUTOMATED EIA MICROPLATE READER EL310

K-Number: K842085 · 1984-06-11

ApplicantBio-Tek Instruments, Inc.
Decision Date1984-06-11
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AUTOMATED EIA MICROPLATE READER EL310 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 1984-06-11 under 510(k) number K842085. 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 EL310?

AUTOMATED EIA MICROPLATE READER EL310 is a medical device that received FDA 510(k) clearance on 1984-06-11. The listed applicant is Bio-Tek Instruments, Inc.. The 510(k) number is K842085.

When did AUTOMATED EIA MICROPLATE READER EL310 receive FDA 510(k) clearance?

AUTOMATED EIA MICROPLATE READER EL310 received FDA 510(k) clearance on 1984-06-11, under 510(k) number K842085.

Who is the listed applicant for AUTOMATED EIA MICROPLATE READER EL310?

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 EL310?

The FDA product code for AUTOMATED EIA MICROPLATE READER EL310 is JJQ.

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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.

K973609IDA-4 AND IPT-MCK971273INDEX 2E, INDEX 2F, INDEX 2EF, CARDIOSAT 100E, CARDIOSAT 100F, CARDIOSAT 100EFK961862MODELS IDA-2 PLUS AND IPT-1K954391MODELS QED-6, 6M AND 6H DEFIBRILLATOR ANALYZER WITH OPTIONAL UNIVERSAL PACEMAKER LOAD ADAPTERK953710ELX808 AUTOMATED MICROPLATE READERSK953572ELX800UV

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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.

K013371UBIT-IR300 INFRARED SPECTROMETRY SYSTEMOtsuka Pharmaceutical Co., Ltd.K980120DIGENE DML 2000 MICROPLATE LUMINOMETERDigene Corp.K973938ALPHA 4 LS AUTOMATED MICROTITERPLATE PROCESSOR AND READERSfri, Inc.K974762STAT TRACKSAwareness Technology, Inc.K962113ANTHOS PHACTS VERSION MICROPLATE READERColumbia Bioscience, Inc.K961183CBI 7520 READERColumbia Bioscience, 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.

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