ABBOTT AXSYM MYOGLOBIN
K-Number: K983848 · 1998-11-16
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Device Summary
Frequently Asked Questions
What is the ABBOTT AXSYM MYOGLOBIN?
ABBOTT AXSYM MYOGLOBIN is a medical device that received FDA 510(k) clearance on 1998-11-16. The listed applicant is Abbott Laboratories. The 510(k) number is K983848.
When did ABBOTT AXSYM MYOGLOBIN receive FDA 510(k) clearance?
ABBOTT AXSYM MYOGLOBIN received FDA 510(k) clearance on 1998-11-16, under 510(k) number K983848.
Who is the listed applicant for ABBOTT AXSYM MYOGLOBIN?
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 AXSYM MYOGLOBIN?
The FDA product code for ABBOTT AXSYM MYOGLOBIN is DDR.
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: DDR)
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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