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FDA 510(k)

MODUMATIC (R) DILUTER

K-Number: K861640 · 1986-05-23

ApplicantTri-Continent Scientific, Inc.
Decision Date1986-05-23
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MODUMATIC (R) DILUTER is the device name listed in this FDA 510(k) record. The listed applicant is Tri-Continent Scientific, Inc.. It received FDA 510(k) clearance on 1986-05-23 under 510(k) number K861640. 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 MODUMATIC (R) DILUTER?

MODUMATIC (R) DILUTER is a medical device that received FDA 510(k) clearance on 1986-05-23. The listed applicant is Tri-Continent Scientific, Inc.. The 510(k) number is K861640.

When did MODUMATIC (R) DILUTER receive FDA 510(k) clearance?

MODUMATIC (R) DILUTER received FDA 510(k) clearance on 1986-05-23, under 510(k) number K861640.

Who is the listed applicant for MODUMATIC (R) DILUTER?

The FDA 510(k) record lists Tri-Continent Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODUMATIC (R) DILUTER?

The FDA product code for MODUMATIC (R) DILUTER 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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