Sechrist Industries, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBER, SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBER, MODEL 3300E/ER MONOPLACE HYPERBARIC OXYGEN CHAMBER
23
Total
22
Cleared
0
Denied
FDA 510(k) Regulatory Record - Sechrist Industries, Inc. General Hospital ✕
1 devices