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FDA 510(k)

NOVAPATH SP ADVANCED LIQUID HANDLING SYSTEM

K-Number: K900775 · 1990-03-09

ApplicantBio-Rad
Decision Date1990-03-09
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

NOVAPATH SP ADVANCED LIQUID HANDLING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1990-03-09 under 510(k) number K900775. 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 NOVAPATH SP ADVANCED LIQUID HANDLING SYSTEM?

NOVAPATH SP ADVANCED LIQUID HANDLING SYSTEM is a medical device that received FDA 510(k) clearance on 1990-03-09. The listed applicant is Bio-Rad. The 510(k) number is K900775.

When did NOVAPATH SP ADVANCED LIQUID HANDLING SYSTEM receive FDA 510(k) clearance?

NOVAPATH SP ADVANCED LIQUID HANDLING SYSTEM received FDA 510(k) clearance on 1990-03-09, under 510(k) number K900775.

Who is the listed applicant for NOVAPATH SP ADVANCED LIQUID HANDLING SYSTEM?

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

What is the FDA product code for NOVAPATH SP ADVANCED LIQUID HANDLING SYSTEM?

The FDA product code for NOVAPATH SP ADVANCED LIQUID HANDLING SYSTEM is JQW.

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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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