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FDA 510(k)

PIPETTE 12 CHANNEL

K-Number: K831644 · 1983-08-01

ApplicantOrganon Teknika Corp.
Decision Date1983-08-01
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PIPETTE 12 CHANNEL 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 1983-08-01 under 510(k) number K831644. The device is classified under product code JTC. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PIPETTE 12 CHANNEL?

PIPETTE 12 CHANNEL is a medical device that received FDA 510(k) clearance on 1983-08-01. The listed applicant is Organon Teknika Corp.. The 510(k) number is K831644.

When did PIPETTE 12 CHANNEL receive FDA 510(k) clearance?

PIPETTE 12 CHANNEL received FDA 510(k) clearance on 1983-08-01, under 510(k) number K831644.

Who is the listed applicant for PIPETTE 12 CHANNEL?

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 PIPETTE 12 CHANNEL?

The FDA product code for PIPETTE 12 CHANNEL is JTC.

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Other records listing Organon Teknika Corp. as applicant

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Related Devices (Code: JTC)

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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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