MICROLAB 4000, MICROLAB 4200
K-Number: K961896 · 1996-08-16
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Device Summary
Frequently Asked Questions
What is the MICROLAB 4000, MICROLAB 4200?
MICROLAB 4000, MICROLAB 4200 is a medical device that received FDA 510(k) clearance on 1996-08-16. The listed applicant is Hamilton Co.. The 510(k) number is K961896.
When did MICROLAB 4000, MICROLAB 4200 receive FDA 510(k) clearance?
MICROLAB 4000, MICROLAB 4200 received FDA 510(k) clearance on 1996-08-16, under 510(k) number K961896.
Who is the listed applicant for MICROLAB 4000, MICROLAB 4200?
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 4000, MICROLAB 4200?
The FDA product code for MICROLAB 4000, MICROLAB 4200 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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