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FDA 510(k)

GENETIC SYSTEMS PIPETTOR/DILUTOR

K-Number: K891765 · 1989-05-01

Decision Date1989-05-01
Product CodeJTC
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

GENETIC SYSTEMS PIPETTOR/DILUTOR is the device name listed in this FDA 510(k) record. The listed applicant is Genetic Systems Corp.. It received FDA 510(k) clearance on 1989-05-01 under 510(k) number K891765. 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 GENETIC SYSTEMS PIPETTOR/DILUTOR?

GENETIC SYSTEMS PIPETTOR/DILUTOR is a medical device that received FDA 510(k) clearance on 1989-05-01. The listed applicant is Genetic Systems Corp.. The 510(k) number is K891765.

When did GENETIC SYSTEMS PIPETTOR/DILUTOR receive FDA 510(k) clearance?

GENETIC SYSTEMS PIPETTOR/DILUTOR received FDA 510(k) clearance on 1989-05-01, under 510(k) number K891765.

Who is the listed applicant for GENETIC SYSTEMS PIPETTOR/DILUTOR?

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

What is the FDA product code for GENETIC SYSTEMS PIPETTOR/DILUTOR?

The FDA product code for GENETIC SYSTEMS PIPETTOR/DILUTOR is JTC.

Related Clinical Trials

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.

Other records listing Genetic Systems 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.

View all 12 devices →

Related Devices (Code: JTC)

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.

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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