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FDA 510(k)

DIGITAL DISPENSING PUMP

K-Number: K810509 · 1981-03-06

ApplicantDynatech Corp.
Decision Date1981-03-06
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DIGITAL DISPENSING PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Dynatech Corp.. It received FDA 510(k) clearance on 1981-03-06 under 510(k) number K810509. 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 DIGITAL DISPENSING PUMP?

DIGITAL DISPENSING PUMP is a medical device that received FDA 510(k) clearance on 1981-03-06. The listed applicant is Dynatech Corp.. The 510(k) number is K810509.

When did DIGITAL DISPENSING PUMP receive FDA 510(k) clearance?

DIGITAL DISPENSING PUMP received FDA 510(k) clearance on 1981-03-06, under 510(k) number K810509.

Who is the listed applicant for DIGITAL DISPENSING PUMP?

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

What is the FDA product code for DIGITAL DISPENSING PUMP?

The FDA product code for DIGITAL DISPENSING PUMP is JQW.

Related Clinical Trials

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Other records listing Dynatech Corp. 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.

K904567DYNATECH MR4000 MICROPLATE READERK854603MULTI MASH 2000K854602MINI MASH 2000K854604AUTO MASHK832117IMMULON SUBSTRATE REMOVAWELL STRIPSK823787HANDI-WASH

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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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