VOLUME TEST DYE 6
K-Number: K841422 · 1984-05-11
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Device Summary
Frequently Asked Questions
What is the VOLUME TEST DYE 6?
VOLUME TEST DYE 6 is a medical device that received FDA 510(k) clearance on 1984-05-11. The listed applicant is Reagent Laboratory, Inc.. The 510(k) number is K841422.
When did VOLUME TEST DYE 6 receive FDA 510(k) clearance?
VOLUME TEST DYE 6 received FDA 510(k) clearance on 1984-05-11, under 510(k) number K841422.
Who is the listed applicant for VOLUME TEST DYE 6?
The FDA 510(k) record lists Reagent Laboratory, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VOLUME TEST DYE 6?
The FDA product code for VOLUME TEST DYE 6 is JJO.
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 Reagent Laboratory, Inc. 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: JJO)
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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