AUTO EIA MICROPLATE READ MODEL CERES 900 W/VAR OPT
K-Number: K914906 · 1991-11-27
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Device Summary
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.
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
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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