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FDA 510(k)

REDY 2000

K-Number: K840743 · 1984-02-06

ApplicantOrganon Teknika Corp.
Decision Date1984-02-06
Product Code
DecisionUnknown

Device Summary

REDY 2000 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 1984-02-06 under 510(k) number K840743. FDA Decision: Unknown.

Frequently Asked Questions

What is the REDY 2000?

REDY 2000 is a medical device that received FDA 510(k) clearance on 1984-02-06. The listed applicant is Organon Teknika Corp.. The 510(k) number is K840743.

When did REDY 2000 receive FDA 510(k) clearance?

REDY 2000 received FDA 510(k) clearance on 1984-02-06, under 510(k) number K840743.

Who is the listed applicant for REDY 2000?

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

Other records listing Organon Teknika Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K003104BACT/ALERT CSRK000492MDA D-DIMERK000378BACT/ALERT MB CULTURE BOTTLEK994343BACT/ALERT SVK993423BACT/ALERT SAK993421BACT/ALERT SN

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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.

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