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/ Oem Medical Div.
Oem Medical Div.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K924570
OEM MULTI-VAC POWERED SUCTION PUMP
August 5, 1993
K925893
OEM MEDICAL ADULT ANESTHESIA BREATHING CIRCUIT
March 12, 1993
K922748
GUEDEL AIRWAY
July 10, 1992
K811855
SKIN SCRUB KITS
July 31, 1981
K761297
MOUTHPIECE SEAL
January 3, 1977