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FDA 510(k)

MULTI-CHANNEL DISCRETE ANALYZER (MDA-180)

K-Number: K924453 · 1992-12-18

ApplicantOrganon Teknika Corp.
Decision Date1992-12-18
Product CodeJPA
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MULTI-CHANNEL DISCRETE ANALYZER (MDA-180) is the device name listed in this FDA 510(k) record. The listed applicant is Organon Teknika Corp.. It received FDA 510(k) clearance on 1992-12-18 under 510(k) number K924453. The device is classified under product code JPA. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-CHANNEL DISCRETE ANALYZER (MDA-180)?

MULTI-CHANNEL DISCRETE ANALYZER (MDA-180) is a medical device that received FDA 510(k) clearance on 1992-12-18. The listed applicant is Organon Teknika Corp.. The 510(k) number is K924453.

When did MULTI-CHANNEL DISCRETE ANALYZER (MDA-180) receive FDA 510(k) clearance?

MULTI-CHANNEL DISCRETE ANALYZER (MDA-180) received FDA 510(k) clearance on 1992-12-18, under 510(k) number K924453.

Who is the listed applicant for MULTI-CHANNEL DISCRETE ANALYZER (MDA-180)?

The FDA 510(k) record lists Organon Teknika Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTI-CHANNEL DISCRETE ANALYZER (MDA-180)?

The FDA product code for MULTI-CHANNEL DISCRETE ANALYZER (MDA-180) is JPA.

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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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