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FDA 510(k)

ROBOTIC SAMPLE PROCESSOR

K-Number: K912036 · 1991-07-26

ApplicantTecan U.S., Ltd.
Decision Date1991-07-26
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ROBOTIC SAMPLE PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Tecan U.S., Ltd.. It received FDA 510(k) clearance on 1991-07-26 under 510(k) number K912036. 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 ROBOTIC SAMPLE PROCESSOR?

ROBOTIC SAMPLE PROCESSOR is a medical device that received FDA 510(k) clearance on 1991-07-26. The listed applicant is Tecan U.S., Ltd.. The 510(k) number is K912036.

When did ROBOTIC SAMPLE PROCESSOR receive FDA 510(k) clearance?

ROBOTIC SAMPLE PROCESSOR received FDA 510(k) clearance on 1991-07-26, under 510(k) number K912036.

Who is the listed applicant for ROBOTIC SAMPLE PROCESSOR?

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

What is the FDA product code for ROBOTIC SAMPLE PROCESSOR?

The FDA product code for ROBOTIC SAMPLE PROCESSOR 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., Ltd. 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.

K933996PROFIBLOTK915492RSP MEGA SAMPLE PROCESSORK910740SLT MICROPLATE WASHERK894126ROBOTIC SAMPLE PROCESSORK854406TECAN ROBOTIC SAMPLE PROCESSOR(RSP) #500

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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