Dryden Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
21
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K880923PATIENT VENTILATOR ISOLATORSeptember 6, 1988
K880769BREATHING CIRCUIT W/HEATED WIREAugust 24, 1988
K882285NONREBREATHING CIRCUITAugust 16, 1988
K873928UNIVERSAL TOURNIQUETOctober 23, 1987
K873927REUSEABLE BREATHING TUBESOctober 20, 1987
K870859BAG-TAIL BLEED VALVEAugust 3, 1987
K871386BREATHING CIRCUITMay 29, 1987
K870858BADGWELL SAMPLING CATHETERMay 14, 1987
K861540DISPOSABLE BERMAN AND GUEDEL AIRWAYSMay 2, 1986
K850644NASOPHARYNGEAL AIRWAY-ROBERTAZZIMarch 21, 1985
K842843DRYDEN SCAVENGER INTERFACE SYSTEMJuly 27, 1984
K842472DRYDEN INFLATABLE MASKJuly 6, 1984
K841455REUSEABLE NON-CONDUCTIVE FIXED YJune 11, 1984
K840431SCRATCH & SNIFF FOR ANESTHESIAMay 14, 1984
K841722MASS SPECTROMETER INTERFACEMay 14, 1984
K841637THREE PORT SENSOR MANIFOLDMay 2, 1984
K840205DRYDEN MINI BACTERIA FILTERFebruary 4, 1984
K833066DRYDEN MINI BACTERIA FILTEROctober 28, 1983
K800155DISPOSAL LITER BREATHING BAGFebruary 21, 1980
K792097DRYDEN BACTERIA FILTERNovember 13, 1979