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Zefon Medical Products

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K940220REBREATHER BAGSMay 27, 1994
K934462ADULT ANESTHESIA BREATHING CIRCUIT KITSMarch 1, 1994
K930957ZEFON GAS SAMPLING LINESJuly 2, 1993
K924889ZEFON ADULT ANESTHESIA BREATHING CIRCUITMarch 19, 1993