ABBOTT IMX(TM) D-DIMER
K-Number: K893961 · 1989-08-03
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Device Summary
Frequently Asked Questions
What is the ABBOTT IMX(TM) D-DIMER?
ABBOTT IMX(TM) D-DIMER is a medical device that received FDA 510(k) clearance on 1989-08-03. The listed applicant is Abbott Laboratories. The 510(k) number is K893961.
When did ABBOTT IMX(TM) D-DIMER receive FDA 510(k) clearance?
ABBOTT IMX(TM) D-DIMER received FDA 510(k) clearance on 1989-08-03, under 510(k) number K893961.
Who is the listed applicant for ABBOTT IMX(TM) D-DIMER?
The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ABBOTT IMX(TM) D-DIMER?
The FDA product code for ABBOTT IMX(TM) D-DIMER is GHH.
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 Abbott Laboratories 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: GHH)
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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