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FDA 510(k)

BAYER ADVIA 1650 SPECIAL CHEMISTRY CONTROL

K-Number: K030801 · 2003-04-09

Decision Date2003-04-09
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BAYER ADVIA 1650 SPECIAL CHEMISTRY CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Bayer Healthcare, LLC. It received FDA 510(k) clearance on 2003-04-09 under 510(k) number K030801. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BAYER ADVIA 1650 SPECIAL CHEMISTRY CONTROL?

BAYER ADVIA 1650 SPECIAL CHEMISTRY CONTROL is a medical device that received FDA 510(k) clearance on 2003-04-09. The listed applicant is Bayer Healthcare, LLC. The 510(k) number is K030801.

When did BAYER ADVIA 1650 SPECIAL CHEMISTRY CONTROL receive FDA 510(k) clearance?

BAYER ADVIA 1650 SPECIAL CHEMISTRY CONTROL received FDA 510(k) clearance on 2003-04-09, under 510(k) number K030801.

Who is the listed applicant for BAYER ADVIA 1650 SPECIAL CHEMISTRY CONTROL?

The FDA 510(k) record lists Bayer Healthcare, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BAYER ADVIA 1650 SPECIAL CHEMISTRY CONTROL?

The FDA product code for BAYER ADVIA 1650 SPECIAL CHEMISTRY CONTROL is JJY.

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 Bayer Healthcare, LLC 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.

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Related Devices (Code: JJY)

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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