I.V. DRIP MONITOR ALARM DEVICE, MONIFLO— 510(k) K760931

Name: FDA 510(k) clearance K760931
Creator: U.S. Food and Drug Administration
Published: 1977-01-05

Substantially Equivalent

Diemolding Corp.

FDA 510(k) clearance K760931 for I.V. DRIP MONITOR ALARM DEVICE, MONIFLO, Substantially Equivalent on 1977-01-05. Applicant: Diemolding Corp.. Device class: 2.

Clearance details

Applicant: Diemolding Corp.
Product code: Code FLN
Device class: Class 2
Regulation: 21 CFR 880.2420
Advisory panel: General Hospital
Date received: 1976-10-29
Decision date: 1977-01-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FLN

view all

K172242 — DripAssist Plus2018-05-25
K150687 — DripAssist2015-10-13
K133870 — FLUID LEVEL MONITOR2014-04-24
K080704 — LOW FLUID ALARM2008-04-17
K050783 — ISSYS DRUG FLOW MONITOR2006-02-22

More clearances from Diemolding Corp.

view all

K962749 — THERAPEP W/MOUTHPIECE, W/PEDIATRIC MASK, W/SMALL MASK, W/LARGE MASK, RESISTOR/PORT/MOUTHPIECE, RESISTOR/PORT1996-10-10
K961455 — MEDSHIELD/AEROCHAMBER1996-07-25
K902713 — ACCESS. KIT FOR THE BIOSURGE SYNCHRONOUS AUTOTRANS1990-07-25
K902114 — CUFF-MATE 2 ENDOTRACHEAL CUFF INFLATOR & MONITOR1990-07-18
K900754 — RESPIREX 21990-03-15

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