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Esp Plastics, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K821310
ESPREE' ANESTHESIA BACTERIAL FILTER
June 11, 1982
K821311
ESPREE' BREATHING CIRCUIT (W/ACCESS
May 21, 1982
K821309
ESPREE', BREATHING BAG
May 21, 1982
K821308
ESPREE' GUEDEL ESPREE BERMAN AIRWAY
May 21, 1982