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Mahe Intl., Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K030857MAHE PEDIATRIC NASO PHARYNGOSCOPE ITS ASSOCIATED AND ANCILLARY EQUIPMENT AND ENDOSCOPIC ACCESSORIESOctober 16, 2003
K991426MAHE INSTRUMENTSAugust 5, 1999
K942823MAHE INSTRUMENTSDecember 5, 1994