TOTAL BILIRUBIN TEST CATALOG NO. SR1007
K-Number: K885284 · 1989-01-30
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Device Summary
Frequently Asked Questions
What is the TOTAL BILIRUBIN TEST CATALOG NO. SR1007?
TOTAL BILIRUBIN TEST CATALOG NO. SR1007 is a medical device that received FDA 510(k) clearance on 1989-01-30. The listed applicant is Em Diagnostic Systems, Inc.. The 510(k) number is K885284.
When did TOTAL BILIRUBIN TEST CATALOG NO. SR1007 receive FDA 510(k) clearance?
TOTAL BILIRUBIN TEST CATALOG NO. SR1007 received FDA 510(k) clearance on 1989-01-30, under 510(k) number K885284.
Who is the listed applicant for TOTAL BILIRUBIN TEST CATALOG NO. SR1007?
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 TOTAL BILIRUBIN TEST CATALOG NO. SR1007?
The FDA product code for TOTAL BILIRUBIN TEST CATALOG NO. SR1007 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.
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