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FDA 510(k)

4 CHANNEL DISPENSER

K-Number: K944556 · 1994-10-25

ApplicantTecan U.S., Inc.
Decision Date1994-10-25
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

4 CHANNEL DISPENSER is the device name listed in this FDA 510(k) record. The listed applicant is Tecan U.S., Inc.. It received FDA 510(k) clearance on 1994-10-25 under 510(k) number K944556. 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 4 CHANNEL DISPENSER?

4 CHANNEL DISPENSER is a medical device that received FDA 510(k) clearance on 1994-10-25. The listed applicant is Tecan U.S., Inc.. The 510(k) number is K944556.

When did 4 CHANNEL DISPENSER receive FDA 510(k) clearance?

4 CHANNEL DISPENSER received FDA 510(k) clearance on 1994-10-25, under 510(k) number K944556.

Who is the listed applicant for 4 CHANNEL DISPENSER?

The FDA 510(k) record lists Tecan U.S., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 4 CHANNEL DISPENSER?

The FDA product code for 4 CHANNEL DISPENSER 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Tecan U.S., Inc. 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.

K963268GENESIS RMPK953345GENESISK9426554 CHANNEL DISPENSER

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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