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FDA 510(k)

MICROPLATE PROCESSOR 3000

K-Number: K945135 · 1995-03-03

ApplicantOrganon Teknika Corp.
Decision Date1995-03-03
Product CodeJJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MICROPLATE PROCESSOR 3000 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 1995-03-03 under 510(k) number K945135. The device is classified under product code JJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROPLATE PROCESSOR 3000?

MICROPLATE PROCESSOR 3000 is a medical device that received FDA 510(k) clearance on 1995-03-03. The listed applicant is Organon Teknika Corp.. The 510(k) number is K945135.

When did MICROPLATE PROCESSOR 3000 receive FDA 510(k) clearance?

MICROPLATE PROCESSOR 3000 received FDA 510(k) clearance on 1995-03-03, under 510(k) number K945135.

Who is the listed applicant for MICROPLATE PROCESSOR 3000?

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 MICROPLATE PROCESSOR 3000?

The FDA product code for MICROPLATE PROCESSOR 3000 is JJE.

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Related Devices (Code: JJE)

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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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