Inmed Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
32
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K862672ESOPHAGEAL STETHOSCOPE WITH THERMISTOROctober 27, 1986
K853162STERILE NASOPHARYNGEAL AIRWAYAugust 6, 1985
K850248DISPOSABLE GUEDEL AIRWAYMarch 12, 1985
K850152PRECONNECTED URETHRAL CATHETER TRAYMarch 12, 1985
K850335URETEROSCOPY CATHETERMarch 12, 1985
K844801ULTRA EXTERNAL CATHETERJanuary 15, 1985
K842301DISPOSABLE LATEX BANDAGENovember 5, 1984
K842866URETHRAL CATHETERIZATION TRAYSeptember 10, 1984
K841040FOX POST NASAL BALLOON CATHETERAugust 17, 1984
K842865ESOPHAGEAL STETHOSCOPEAugust 15, 1984
K841037PENROSE DRAINSApril 25, 1984
K841033MILLER-ABBOTT TUBEApril 13, 1984
K841038BLAKEMORE TUBEApril 13, 1984
K841035ULTRA BAKER JEJUNOSTOMY TUBEApril 13, 1984
K841039CANTOR TUBEApril 13, 1984
K841034DEAVER T-DRAIN & CATTEL T-DRAINApril 13, 1984
K841036RECTAL BALLOON CATHETERSApril 13, 1984
K840973COLE TUBE-LATEXMarch 30, 1984
K841093NASOPHARYNGEAL AIRWAYSMarch 23, 1984
K832363FOLEY CATHETERIZATION TRAY-VARIOUSMarch 7, 1984