MODUMATIC (R) DILUTER— 510(k) K861640

Name: FDA 510(k) clearance K861640
Creator: U.S. Food and Drug Administration
Published: 1986-05-23

Substantially Equivalent

Tri-Continent Scientific, Inc.

FDA 510(k) clearance K861640 for MODUMATIC (R) DILUTER, Substantially Equivalent on 1986-05-23. Applicant: Tri-Continent Scientific, Inc.. Device class: 1.

Clearance details

Applicant: Tri-Continent Scientific, Inc.
Product code: Code JQW
Device class: Class 1
Regulation: 21 CFR 862.2750
Advisory panel: Clinical Chemistry
Date received: 1986-04-30
Decision date: 1986-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Grass Valley, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JQW

view all

K023955 — BD VIPER INSTRUMENT2003-06-24
K973335 — QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)1998-04-30
K980180 — 2700 SAMPLE MANAGER1998-02-12
K970420 — MASTERCAP AM 5.0/MASTERCAP RM 5.01997-06-30
K970616 — MINI SAMPLER PROCESSOR1997-04-21

Data sourced from openFDA. This site is unofficial and independent of the FDA.