FDA 510(k)

HIGH SPEED DISPENSER

K-Number: K840938 · 1984-04-19

Decision Date1984-04-19

Product CodeJQW

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

HIGH SPEED DISPENSER is the device name listed in this FDA 510(k) record. The listed applicant is Micromedic Systems. It received FDA 510(k) clearance on 1984-04-19 under 510(k) number K840938. 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 HIGH SPEED DISPENSER?

HIGH SPEED DISPENSER is a medical device that received FDA 510(k) clearance on 1984-04-19. The listed applicant is Micromedic Systems. The 510(k) number is K840938.

When did HIGH SPEED DISPENSER receive FDA 510(k) clearance?

HIGH SPEED DISPENSER received FDA 510(k) clearance on 1984-04-19, under 510(k) number K840938.

Who is the listed applicant for HIGH SPEED DISPENSER?

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

What is the FDA product code for HIGH SPEED DISPENSER?

The FDA product code for HIGH SPEED 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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Micromedic Systems as applicant

K923643MEDICOOL K872309MICROMEDIC COMBOSTAT LH/FSH KIT K871008MICROMEDIC NEONATAL T4 KIT K870904MICROMEDIC NEONATAL TSH MONOCLONAL IRMA KIT K871505AUTOPAK NEONATAL TSH MONOCLONAL IRMA KIT K870245AUTOPAK TSH MONOCLONAL IRMA KIT

View all 42 devices →

Related Devices (Code: JQW)

K023955BD VIPER INSTRUMENTBecton, Dickinson & CO K973335QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)Zenyx Scientific , Ltd.K9801802700 SAMPLE MANAGERWaters Corporation K970420MASTERCAP 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.