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FDA 510(k)

MICROPLATE AUTO-WASHER (MOTORIZED STAGE)

K-Number: K873542 · 1987-09-23

Decision Date1987-09-23
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MICROPLATE AUTO-WASHER (MOTORIZED STAGE) is the device name listed in this FDA 510(k) record. The listed applicant is Genetic Systems Corp.. It received FDA 510(k) clearance on 1987-09-23 under 510(k) number K873542. The device is classified under product code JTC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROPLATE AUTO-WASHER (MOTORIZED STAGE)?

MICROPLATE AUTO-WASHER (MOTORIZED STAGE) is a medical device that received FDA 510(k) clearance on 1987-09-23. The listed applicant is Genetic Systems Corp.. The 510(k) number is K873542.

When did MICROPLATE AUTO-WASHER (MOTORIZED STAGE) receive FDA 510(k) clearance?

MICROPLATE AUTO-WASHER (MOTORIZED STAGE) received FDA 510(k) clearance on 1987-09-23, under 510(k) number K873542.

Who is the listed applicant for MICROPLATE AUTO-WASHER (MOTORIZED STAGE)?

The FDA 510(k) record lists Genetic Systems Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROPLATE AUTO-WASHER (MOTORIZED STAGE)?

The FDA product code for MICROPLATE AUTO-WASHER (MOTORIZED STAGE) is JTC.

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 Genetic Systems Corp. 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 12 devices →

Related Devices (Code: JTC)

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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