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FDA 510(k)

DIMENSION VISTA ENZYME 1 CALIBRATOR (ENZ 1 CAL - KC310)

K-Number: K061923 · 2006-08-25

Decision Date2006-08-25
Product CodeJIX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DIMENSION VISTA ENZYME 1 CALIBRATOR (ENZ 1 CAL - KC310) is the device name listed in this FDA 510(k) record. The listed applicant is Dade Behring, Inc.. It received FDA 510(k) clearance on 2006-08-25 under 510(k) number K061923. 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 DIMENSION VISTA ENZYME 1 CALIBRATOR (ENZ 1 CAL - KC310)?

DIMENSION VISTA ENZYME 1 CALIBRATOR (ENZ 1 CAL - KC310) is a medical device that received FDA 510(k) clearance on 2006-08-25. The listed applicant is Dade Behring, Inc.. The 510(k) number is K061923.

When did DIMENSION VISTA ENZYME 1 CALIBRATOR (ENZ 1 CAL - KC310) receive FDA 510(k) clearance?

DIMENSION VISTA ENZYME 1 CALIBRATOR (ENZ 1 CAL - KC310) received FDA 510(k) clearance on 2006-08-25, under 510(k) number K061923.

Who is the listed applicant for DIMENSION VISTA ENZYME 1 CALIBRATOR (ENZ 1 CAL - KC310)?

The FDA 510(k) record lists Dade Behring, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIMENSION VISTA ENZYME 1 CALIBRATOR (ENZ 1 CAL - KC310)?

The FDA product code for DIMENSION VISTA ENZYME 1 CALIBRATOR (ENZ 1 CAL - KC310) 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 Dade Behring, 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 343 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

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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