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FDA 510(k)

AUTO EIA MICROPLATE READ MODEL CERES 900 W/VAR OPT

K-Number: K914906 · 1991-11-27

Decision Date1991-11-27
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AUTO EIA MICROPLATE READ MODEL CERES 900 W/VAR OPT 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 1991-11-27 under 510(k) number K914906. 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 AUTO EIA MICROPLATE READ MODEL CERES 900 W/VAR OPT?

AUTO EIA MICROPLATE READ MODEL CERES 900 W/VAR OPT is a medical device that received FDA 510(k) clearance on 1991-11-27. The listed applicant is Bio-Tek Instruments, Inc.. The 510(k) number is K914906.

When did AUTO EIA MICROPLATE READ MODEL CERES 900 W/VAR OPT receive FDA 510(k) clearance?

AUTO EIA MICROPLATE READ MODEL CERES 900 W/VAR OPT received FDA 510(k) clearance on 1991-11-27, under 510(k) number K914906.

Who is the listed applicant for AUTO EIA MICROPLATE READ MODEL CERES 900 W/VAR OPT?

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 AUTO EIA MICROPLATE READ MODEL CERES 900 W/VAR OPT?

The FDA product code for AUTO EIA MICROPLATE READ MODEL CERES 900 W/VAR OPT 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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