FILTER, VACUUM LINE LINEGUARD— 510(k) K760420

Substantially Equivalent

Diemolding Corp.

FDA 510(k) clearance K760420 for FILTER, VACUUM LINE LINEGUARD, Substantially Equivalent on 1976-08-23. Applicant: Diemolding Corp.. Device class: 2.

Clearance details

Applicant: Diemolding Corp.
Product code: Code KPQ
Device class: Class 2
Regulation: 21 CFR 892.5840
Advisory panel: Radiology
Date received: 1976-08-06
Decision date: 1976-08-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KPQ

K132944 — ADVANTAGESIM MD MR PELVIC ORGAN AT RISK SEGMENTATION2014-03-14
K132045 — ADVANTAGESIM MD WITH CT ATLAS-BASED CONTOURING AND RE-PLANNING OPTIONS2013-09-04
K101038 — RAD II SIMULATOR, RAD II KV IMAGER, DUAL RAD II KV IMAGER2010-08-17
K090706 — ONCENTRA SIMULATION 2.32009-06-15
K083591 — IKOENGELO, VERSION 22008-12-29

More clearances from Diemolding Corp.

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.