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Arch Development Group

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K913047STERILESERT(TM) CABLE AND POLE DRAPEOctober 2, 1991
K912765STASIS BUTTON PRSSURE DEVICEAugust 12, 1991