DIGOXIN IMMUNOASSAY
K-Number: K983323 · 1998-11-12
Advertisement
Device Summary
Frequently Asked Questions
What is the DIGOXIN IMMUNOASSAY?
DIGOXIN IMMUNOASSAY is a medical device that received FDA 510(k) clearance on 1998-11-12. The listed applicant is Diagnostic Reagents, Inc.. The 510(k) number is K983323.
When did DIGOXIN IMMUNOASSAY receive FDA 510(k) clearance?
DIGOXIN IMMUNOASSAY received FDA 510(k) clearance on 1998-11-12, under 510(k) number K983323.
Who is the listed applicant for DIGOXIN IMMUNOASSAY?
The FDA 510(k) record lists Diagnostic Reagents, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIGOXIN IMMUNOASSAY?
The FDA product code for DIGOXIN IMMUNOASSAY is KXT.
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 Diagnostic Reagents, 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: KXT)
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.
Advertisement