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FDA 510(k)

MINI-DILUTER 2

K-Number: K782130 · 1979-02-15

ApplicantDynatech Laboratories, Inc.
Decision Date1979-02-15
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MINI-DILUTER 2 is the device name listed in this FDA 510(k) record. The listed applicant is Dynatech Laboratories, Inc.. It received FDA 510(k) clearance on 1979-02-15 under 510(k) number K782130. 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 MINI-DILUTER 2?

MINI-DILUTER 2 is a medical device that received FDA 510(k) clearance on 1979-02-15. The listed applicant is Dynatech Laboratories, Inc.. The 510(k) number is K782130.

When did MINI-DILUTER 2 receive FDA 510(k) clearance?

MINI-DILUTER 2 received FDA 510(k) clearance on 1979-02-15, under 510(k) number K782130.

Who is the listed applicant for MINI-DILUTER 2?

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

What is the FDA product code for MINI-DILUTER 2?

The FDA product code for MINI-DILUTER 2 is JQW.

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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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