SYSTEMATE DIRECT BILIRUBIN TEST TECHNICON RA 1000
K-Number: K922856 · 1992-09-09
Advertisement
Device Summary
Frequently Asked Questions
What is the SYSTEMATE DIRECT BILIRUBIN TEST TECHNICON RA 1000?
SYSTEMATE DIRECT BILIRUBIN TEST TECHNICON RA 1000 is a medical device that received FDA 510(k) clearance on 1992-09-09. The listed applicant is Em Diagnostic Systems, Inc.. The 510(k) number is K922856.
When did SYSTEMATE DIRECT BILIRUBIN TEST TECHNICON RA 1000 receive FDA 510(k) clearance?
SYSTEMATE DIRECT BILIRUBIN TEST TECHNICON RA 1000 received FDA 510(k) clearance on 1992-09-09, under 510(k) number K922856.
Who is the listed applicant for SYSTEMATE DIRECT BILIRUBIN TEST TECHNICON RA 1000?
The FDA 510(k) record lists Em Diagnostic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYSTEMATE DIRECT BILIRUBIN TEST TECHNICON RA 1000?
The FDA product code for SYSTEMATE DIRECT BILIRUBIN TEST TECHNICON RA 1000 is CIG.
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 Em Diagnostic Systems, 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: CIG)
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