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FDA 510(k)

PIPETTOR, 400, CENTRIFICHEM SYSTEM

K-Number: K770193 · 1977-03-01

ApplicantUniversal Instruments Corp.
Decision Date1977-03-01
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PIPETTOR, 400, CENTRIFICHEM SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Universal Instruments Corp.. It received FDA 510(k) clearance on 1977-03-01 under 510(k) number K770193. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PIPETTOR, 400, CENTRIFICHEM SYSTEM?

PIPETTOR, 400, CENTRIFICHEM SYSTEM is a medical device that received FDA 510(k) clearance on 1977-03-01. The listed applicant is Universal Instruments Corp.. The 510(k) number is K770193.

When did PIPETTOR, 400, CENTRIFICHEM SYSTEM receive FDA 510(k) clearance?

PIPETTOR, 400, CENTRIFICHEM SYSTEM received FDA 510(k) clearance on 1977-03-01, under 510(k) number K770193.

Who is the listed applicant for PIPETTOR, 400, CENTRIFICHEM SYSTEM?

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

What is the FDA product code for PIPETTOR, 400, CENTRIFICHEM SYSTEM?

The FDA product code for PIPETTOR, 400, CENTRIFICHEM SYSTEM is JQW.

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.

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Other records listing Universal Instruments 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.

K833024OFTALMOGRAF

Related Devices (Code: JQW)

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.

K023955BD VIPER INSTRUMENTBecton, Dickinson & COK973335QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)Zenyx Scientific , Ltd.K9801802700 SAMPLE MANAGERWaters CorporationK970420MASTERCAP AM 5.0/MASTERCAP RM 5.0Pharmacia, Inc.K970616MINI SAMPLER PROCESSORCavro Scientific Instruments, Inc.K962687GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEMNichols Institute Diagnostics

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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