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Mellen Air Mfg., Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K963510APREMA I - ALTERNATING PRESSURE AIR FLOTATION MATTRESS SYSTEMNovember 26, 1996
K961129AREMA IIApril 17, 1996