MODIFIED AEROCHAMBER M.V. AEROSOL HOLDING CHAMBER— 510(k) K900557

Name: FDA 510(k) clearance K900557
Creator: U.S. Food and Drug Administration
Published: 1991-04-10

Substantially Equivalent

Monaghan Medical Corp.

FDA 510(k) clearance K900557 for MODIFIED AEROCHAMBER M.V. AEROSOL HOLDING CHAMBER, Substantially Equivalent on 1991-04-10. Applicant: Monaghan Medical Corp.. Device class: 1.

Clearance details

Applicant: Monaghan Medical Corp.
Product code: Code CCQ
Device class: Class 1
Regulation: 21 CFR 868.5640
Advisory panel: Anesthesiology
Date received: 1990-02-07
Decision date: 1991-04-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Plattsburgh, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code CCQ

view all

K972397 — EZ SPRAY1997-09-23
K964956 — E-Z SPACER MASK (SMALL)1997-04-23
K961894 — MDI TUTOR1996-08-14
K961455 — MEDSHIELD/AEROCHAMBER1996-07-25
K960593 — SMARTMIST ASTHMA MANAGMENT SYSTEM, SMARTMIST, MODEL NUMBER SM-100/SMARTMIST SPIROMETRY AIRWAY, MODEL NUMBER SA-1001996-05-10

More clearances from Monaghan Medical Corp.

view all

K123945 — STRIVE DUAL ZONE PEAK FLOW METER2013-04-17
K031514 — MODIFICATION TO TRUPEAK PEAK FLOW METER2003-05-23
K023097 — TRUEZONE PEAK FLOW METER2003-03-07
K012939 — AEROVENT II CHC COLLAPSIBLE HOLDING CHAMBER2001-09-28
K991212 — MODIFICATION TO TRUZONE PEAK FLOW METER1999-07-01

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