MICROLAB M-MICROPROCESSOR DILUTER/DISP
K-Number: K801913 · 1980-09-26
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Device Summary
Frequently Asked Questions
What is the MICROLAB M-MICROPROCESSOR DILUTER/DISP?
MICROLAB M-MICROPROCESSOR DILUTER/DISP is a medical device that received FDA 510(k) clearance on 1980-09-26. The listed applicant is Hamilton Co.. The 510(k) number is K801913.
When did MICROLAB M-MICROPROCESSOR DILUTER/DISP receive FDA 510(k) clearance?
MICROLAB M-MICROPROCESSOR DILUTER/DISP received FDA 510(k) clearance on 1980-09-26, under 510(k) number K801913.
Who is the listed applicant for MICROLAB M-MICROPROCESSOR DILUTER/DISP?
The FDA 510(k) record lists Hamilton Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICROLAB M-MICROPROCESSOR DILUTER/DISP?
The FDA product code for MICROLAB M-MICROPROCESSOR DILUTER/DISP 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 Hamilton Co. 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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