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FDA 510(k)

PRECISION DISPENSER

K-Number: K843606 · 1984-09-21

ApplicantMedical Technomics, Ltd.
Decision Date1984-09-21
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PRECISION DISPENSER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Technomics, Ltd.. It received FDA 510(k) clearance on 1984-09-21 under 510(k) number K843606. 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 PRECISION DISPENSER?

PRECISION DISPENSER is a medical device that received FDA 510(k) clearance on 1984-09-21. The listed applicant is Medical Technomics, Ltd.. The 510(k) number is K843606.

When did PRECISION DISPENSER receive FDA 510(k) clearance?

PRECISION DISPENSER received FDA 510(k) clearance on 1984-09-21, under 510(k) number K843606.

Who is the listed applicant for PRECISION DISPENSER?

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

What is the FDA product code for PRECISION DISPENSER?

The FDA product code for PRECISION 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.

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Other records listing Medical Technomics, 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.

K844798EPPENDORF DILUTERK843608CAPILLARY BLOOD COLLECTION TUBEK843361MINICAPSK843607LABOPETTORK843362RINGCAPS

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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