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FDA 510(k)

MICROLAB M-MICROPROCESSOR DILUTER/DISP

K-Number: K801913 · 1980-09-26

ApplicantHamilton Co.
Decision Date1980-09-26
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MICROLAB M-MICROPROCESSOR DILUTER/DISP is the device name listed in this FDA 510(k) record. The listed applicant is Hamilton Co.. It received FDA 510(k) clearance on 1980-09-26 under 510(k) number K801913. 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 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.

View all 16 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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