QUANTEX C3
K-Number: K962199 · 1996-09-25
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Device Summary
Frequently Asked Questions
What is the QUANTEX C3?
QUANTEX C3 is a medical device that received FDA 510(k) clearance on 1996-09-25. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K962199.
When did QUANTEX C3 receive FDA 510(k) clearance?
QUANTEX C3 received FDA 510(k) clearance on 1996-09-25, under 510(k) number K962199.
Who is the listed applicant for QUANTEX C3?
The FDA 510(k) record lists Instrumentation Laboratory CO as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QUANTEX C3?
The FDA product code for QUANTEX C3 is CZW.
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 Instrumentation Laboratory 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: CZW)
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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