Monaghan Medical Corp.

FDA Regulatory Profile

Monaghan Medical Corp. appears in FDA public data with 0 recalls, 33 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 17, 2013.

Summary

Total Recalls
0
510(k) Clearances
33
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K123945STRIVE DUAL ZONE PEAK FLOW METERApril 17, 2013
K031514MODIFICATION TO TRUPEAK PEAK FLOW METERMay 23, 2003
K023097TRUEZONE PEAK FLOW METERMarch 7, 2003
K012939AEROVENT II CHC COLLAPSIBLE HOLDING CHAMBERSeptember 28, 2001
K991212MODIFICATION TO TRUZONE PEAK FLOW METERJuly 1, 1999
K964130AEROGEAR ASTHMA ACTION KITJanuary 10, 1997
K963089TRUZONE PEAK FLOW METERNovember 6, 1996
K963095TRUPEAK PEAK FLOW METERNovember 4, 1996
K955234TRUPEAK PEAK FLOW METERMarch 18, 1996
K955262TRUZONE PEAK FLOW METERMarch 7, 1996
K944512TRUZONE PFM DISPOSABLE MOUTHPIECENovember 2, 1994
K930574AEROCHAMBER W/MASK, MODIFIEDJanuary 24, 1994
K926307PEAK FLOW METERJuly 22, 1993
K91126322MM ID/OD ADAPTERAugust 19, 1991
K900576MODIFIED AEROCHAMBER WITH MASKMay 13, 1991
K900557MODIFIED AEROCHAMBER M.V. AEROSOL HOLDING CHAMBERApril 10, 1991
K910138TVS II ELECTRONIC INCENTIVE SPIROMETERMarch 12, 1991
K884389MODIFIED 225/SIMV VOLUME VENTILATORMarch 12, 1990
K894969AEROVENTOctober 30, 1989
K884942MONAGHAN RVM, MODEL 761June 7, 1989