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FDA 510(k)

DIRECT BILIRUBIN TEST CATALOG NO. SR1008

K-Number: K885285 · 1989-01-30

Decision Date1989-01-30
Product CodeCIG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DIRECT BILIRUBIN TEST CATALOG NO. SR1008 is the device name listed in this FDA 510(k) record. The listed applicant is Em Diagnostic Systems, Inc.. It received FDA 510(k) clearance on 1989-01-30 under 510(k) number K885285. The device is classified under product code CIG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIRECT BILIRUBIN TEST CATALOG NO. SR1008?

DIRECT BILIRUBIN TEST CATALOG NO. SR1008 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 K885285.

When did DIRECT BILIRUBIN TEST CATALOG NO. SR1008 receive FDA 510(k) clearance?

DIRECT BILIRUBIN TEST CATALOG NO. SR1008 received FDA 510(k) clearance on 1989-01-30, under 510(k) number K885285.

Who is the listed applicant for DIRECT BILIRUBIN TEST CATALOG NO. SR1008?

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 DIRECT BILIRUBIN TEST CATALOG NO. SR1008?

The FDA product code for DIRECT BILIRUBIN TEST CATALOG NO. SR1008 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.

View all 288 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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