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FDA 510(k)

CALIBRATOR FOR AUTOMATED SYSTEMS

K-Number: K011226 · 2001-06-25

Decision Date2001-06-25
Product CodeJIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CALIBRATOR FOR AUTOMATED SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Roche Diagnostics Corp.. It received FDA 510(k) clearance on 2001-06-25 under 510(k) number K011226. The device is classified under product code JIX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CALIBRATOR FOR AUTOMATED SYSTEMS?

CALIBRATOR FOR AUTOMATED SYSTEMS is a medical device that received FDA 510(k) clearance on 2001-06-25. The listed applicant is Roche Diagnostics Corp.. The 510(k) number is K011226.

When did CALIBRATOR FOR AUTOMATED SYSTEMS receive FDA 510(k) clearance?

CALIBRATOR FOR AUTOMATED SYSTEMS received FDA 510(k) clearance on 2001-06-25, under 510(k) number K011226.

Who is the listed applicant for CALIBRATOR FOR AUTOMATED SYSTEMS?

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?

The FDA product code for CALIBRATOR FOR AUTOMATED SYSTEMS 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.

View all 263 devices →

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

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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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