FDA 510(k)

IMMUNOCYT

K-Number: K994356 · 2000-02-23

Decision Date2000-02-23

Product CodeNBK

Advisory CommitteeHE

DecisionSubstantially Equivalent

Device Summary

IMMUNOCYT is the device name listed in this FDA 510(k) record. The listed applicant is Diagnocure, Inc.. It received FDA 510(k) clearance on 2000-02-23 under 510(k) number K994356. The device is classified under product code NBK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMMUNOCYT?

IMMUNOCYT is a medical device that received FDA 510(k) clearance on 2000-02-23. The listed applicant is Diagnocure, Inc.. The 510(k) number is K994356.

When did IMMUNOCYT receive FDA 510(k) clearance?

IMMUNOCYT received FDA 510(k) clearance on 2000-02-23, under 510(k) number K994356.

Who is the listed applicant for IMMUNOCYT?

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

What is the FDA product code for IMMUNOCYT?

The FDA product code for IMMUNOCYT is NBK.

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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.