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FDA 510(k)

IDS-ISYS IGF-I CALIBRATION VERIFIERS

K-Number: K122141 · 2012-08-07

ApplicantImmunodiagnostic Systems , Ltd.
Decision Date2012-08-07
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

IDS-ISYS IGF-I CALIBRATION VERIFIERS is the device name listed in this FDA 510(k) record. The listed applicant is Immunodiagnostic Systems , Ltd.. It received FDA 510(k) clearance on 2012-08-07 under 510(k) number K122141. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IDS-ISYS IGF-I CALIBRATION VERIFIERS?

IDS-ISYS IGF-I CALIBRATION VERIFIERS is a medical device that received FDA 510(k) clearance on 2012-08-07. The listed applicant is Immunodiagnostic Systems , Ltd.. The 510(k) number is K122141.

When did IDS-ISYS IGF-I CALIBRATION VERIFIERS receive FDA 510(k) clearance?

IDS-ISYS IGF-I CALIBRATION VERIFIERS received FDA 510(k) clearance on 2012-08-07, under 510(k) number K122141.

Who is the listed applicant for IDS-ISYS IGF-I CALIBRATION VERIFIERS?

The FDA 510(k) record lists Immunodiagnostic Systems , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IDS-ISYS IGF-I CALIBRATION VERIFIERS?

The FDA product code for IDS-ISYS IGF-I CALIBRATION VERIFIERS is JJX.

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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.

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