MICROPLATE AUTO-WASHER (MOTORIZED STAGE)
K-Number: K873542 · 1987-09-23
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Device Summary
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.
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
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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