CALIBRATOR FOR AUTOMATED SYSTEMS PROTEINS IN URINE/CSF
K-Number: K040264 · 2004-04-02
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Device Summary
Frequently Asked Questions
What is the CALIBRATOR FOR AUTOMATED SYSTEMS PROTEINS IN URINE/CSF?
CALIBRATOR FOR AUTOMATED SYSTEMS PROTEINS IN URINE/CSF is a medical device that received FDA 510(k) clearance on 2004-04-02. The listed applicant is Roche Diagnostics Corp.. The 510(k) number is K040264.
When did CALIBRATOR FOR AUTOMATED SYSTEMS PROTEINS IN URINE/CSF receive FDA 510(k) clearance?
CALIBRATOR FOR AUTOMATED SYSTEMS PROTEINS IN URINE/CSF received FDA 510(k) clearance on 2004-04-02, under 510(k) number K040264.
Who is the listed applicant for CALIBRATOR FOR AUTOMATED SYSTEMS PROTEINS IN URINE/CSF?
The FDA 510(k) record lists Roche Diagnostics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CALIBRATOR FOR AUTOMATED SYSTEMS PROTEINS IN URINE/CSF?
The FDA product code for CALIBRATOR FOR AUTOMATED SYSTEMS PROTEINS IN URINE/CSF is JIX.
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 Roche Diagnostics Corp. 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: JIX)
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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