Mckesson Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Mckesson Corp. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1976 to 1977. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Mckesson Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Mckesson Corp.
5 devices
Cleared
Aug 02, 1977
RESUSCITATOR, MS30
Anesthesiology
34d
Cleared
Dec 13, 1976
NITROUS OXIDE SCAVENGING MASK
Anesthesiology
7d
Cleared
Dec 09, 1976
HLR QUICK-FIT HEART-LUNG RESUSCITATOR
Cardiovascular
3d
Cleared
Dec 09, 1976
ESOPHAGEAL OBTURATION AIRWAY
Anesthesiology
3d
Cleared
Jul 20, 1976
CONSIOUS SEDATION (ANALOR P-76)
Anesthesiology
39d