DATA CHEM AUTO-BILIRUBIN/DIRECT PROCEDURE
K-Number: K850901 · 1985-04-01
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Device Summary
Frequently Asked Questions
What is the DATA CHEM AUTO-BILIRUBIN/DIRECT PROCEDURE?
DATA CHEM AUTO-BILIRUBIN/DIRECT PROCEDURE is a medical device that received FDA 510(k) clearance on 1985-04-01. The listed applicant is Data Medical Associates, Inc.. The 510(k) number is K850901.
When did DATA CHEM AUTO-BILIRUBIN/DIRECT PROCEDURE receive FDA 510(k) clearance?
DATA CHEM AUTO-BILIRUBIN/DIRECT PROCEDURE received FDA 510(k) clearance on 1985-04-01, under 510(k) number K850901.
Who is the listed applicant for DATA CHEM AUTO-BILIRUBIN/DIRECT PROCEDURE?
The FDA 510(k) record lists Data Medical Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DATA CHEM AUTO-BILIRUBIN/DIRECT PROCEDURE?
The FDA product code for DATA CHEM AUTO-BILIRUBIN/DIRECT PROCEDURE 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 Data Medical Associates, 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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