FDA 510(k)

WIENER LAB. CALIBRATOR A PLUS, MODEL 2X3 ML CAT. NR. 1918006

K-Number: K024305 · 2003-03-18

Decision Date2003-03-18

Product CodeJIX

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

WIENER LAB. CALIBRATOR A PLUS, MODEL 2X3 ML CAT. NR. 1918006 is the device name listed in this FDA 510(k) record. The listed applicant is Wiener Laboratories Saic. It received FDA 510(k) clearance on 2003-03-18 under 510(k) number K024305. 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 WIENER LAB. CALIBRATOR A PLUS, MODEL 2X3 ML CAT. NR. 1918006?

WIENER LAB. CALIBRATOR A PLUS, MODEL 2X3 ML CAT. NR. 1918006 is a medical device that received FDA 510(k) clearance on 2003-03-18. The listed applicant is Wiener Laboratories Saic. The 510(k) number is K024305.

When did WIENER LAB. CALIBRATOR A PLUS, MODEL 2X3 ML CAT. NR. 1918006 receive FDA 510(k) clearance?

WIENER LAB. CALIBRATOR A PLUS, MODEL 2X3 ML CAT. NR. 1918006 received FDA 510(k) clearance on 2003-03-18, under 510(k) number K024305.

Who is the listed applicant for WIENER LAB. CALIBRATOR A PLUS, MODEL 2X3 ML CAT. NR. 1918006?

The FDA 510(k) record lists Wiener Laboratories Saic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WIENER LAB. CALIBRATOR A PLUS, MODEL 2X3 ML CAT. NR. 1918006?

The FDA product code for WIENER LAB. CALIBRATOR A PLUS, MODEL 2X3 ML CAT. NR. 1918006 is JIX.

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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.