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FDA 510(k)

BIOMEK 1000 AUTOMATED LABORATORY WORK STATION

K-Number: K870544 · 1987-04-22

Decision Date1987-04-22
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BIOMEK 1000 AUTOMATED LABORATORY WORK STATION is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Instruments, Inc.. It received FDA 510(k) clearance on 1987-04-22 under 510(k) number K870544. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 281 devices →

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

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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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