BIOMEK 1000 AUTOMATED LABORATORY WORK STATION
K-Number: K870544 · 1987-04-22
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Device Summary
Frequently Asked Questions
What is the BIOMEK 1000 AUTOMATED LABORATORY WORK STATION?
BIOMEK 1000 AUTOMATED LABORATORY WORK STATION is a medical device that received FDA 510(k) clearance on 1987-04-22. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K870544.
When did BIOMEK 1000 AUTOMATED LABORATORY WORK STATION receive FDA 510(k) clearance?
BIOMEK 1000 AUTOMATED LABORATORY WORK STATION received FDA 510(k) clearance on 1987-04-22, under 510(k) number K870544.
Who is the listed applicant for BIOMEK 1000 AUTOMATED LABORATORY WORK STATION?
The FDA 510(k) record lists Beckman Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BIOMEK 1000 AUTOMATED LABORATORY WORK STATION?
The FDA product code for BIOMEK 1000 AUTOMATED LABORATORY WORK STATION is JQW.
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 Beckman 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: JQW)
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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