TECHNICON DAX(TM) SYSTEM
K-Number: K885203 · 1989-03-28
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Device Summary
Frequently Asked Questions
What is the TECHNICON DAX(TM) SYSTEM?
TECHNICON DAX(TM) SYSTEM is a medical device that received FDA 510(k) clearance on 1989-03-28. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K885203.
When did TECHNICON DAX(TM) SYSTEM receive FDA 510(k) clearance?
TECHNICON DAX(TM) SYSTEM received FDA 510(k) clearance on 1989-03-28, under 510(k) number K885203.
Who is the listed applicant for TECHNICON DAX(TM) SYSTEM?
The FDA 510(k) record lists Technicon Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TECHNICON DAX(TM) SYSTEM?
The FDA product code for TECHNICON DAX(TM) SYSTEM is JJG.
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 Technicon Instruments Corp. 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: JJG)
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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