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FDA 510(k)

SYVA IQ 190 DIGITAL PIPETTER DILUTER

K-Number: K842390 · 1984-07-25

ApplicantSyva Co.
Decision Date1984-07-25
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SYVA IQ 190 DIGITAL PIPETTER DILUTER is the device name listed in this FDA 510(k) record. The listed applicant is Syva Co.. It received FDA 510(k) clearance on 1984-07-25 under 510(k) number K842390. 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 SYVA IQ 190 DIGITAL PIPETTER DILUTER?

SYVA IQ 190 DIGITAL PIPETTER DILUTER is a medical device that received FDA 510(k) clearance on 1984-07-25. The listed applicant is Syva Co.. The 510(k) number is K842390.

When did SYVA IQ 190 DIGITAL PIPETTER DILUTER receive FDA 510(k) clearance?

SYVA IQ 190 DIGITAL PIPETTER DILUTER received FDA 510(k) clearance on 1984-07-25, under 510(k) number K842390.

Who is the listed applicant for SYVA IQ 190 DIGITAL PIPETTER DILUTER?

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

What is the FDA product code for SYVA IQ 190 DIGITAL PIPETTER DILUTER?

The FDA product code for SYVA IQ 190 DIGITAL PIPETTER DILUTER is JQW.

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Other records listing Syva Co. as applicant

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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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