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FDA 510(k)

NCS RA LATEX TEST

K-Number: K841146 · 1984-04-20

ApplicantNcs Diagnostics, Inc.
Decision Date1984-04-20
Product CodeDHR
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

NCS RA LATEX TEST is the device name listed in this FDA 510(k) record. The listed applicant is Ncs Diagnostics, Inc.. It received FDA 510(k) clearance on 1984-04-20 under 510(k) number K841146. The device is classified under product code DHR. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NCS RA LATEX TEST?

NCS RA LATEX TEST is a medical device that received FDA 510(k) clearance on 1984-04-20. The listed applicant is Ncs Diagnostics, Inc.. The 510(k) number is K841146.

When did NCS RA LATEX TEST receive FDA 510(k) clearance?

NCS RA LATEX TEST received FDA 510(k) clearance on 1984-04-20, under 510(k) number K841146.

Who is the listed applicant for NCS RA LATEX TEST?

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

What is the FDA product code for NCS RA LATEX TEST?

The FDA product code for NCS RA LATEX TEST is DHR.

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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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