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Mckesson Corp.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K771175	RESUSCITATOR, MS30	BTM	1977-08-02	View
510(k)	K761196	NITROUS OXIDE SCAVENGING MASK	CBN	1976-12-13	View
510(k)	K761195	ESOPHAGEAL OBTURATION AIRWAY	CAO	1976-12-09	View
510(k)	K761194	HLR QUICK-FIT HEART-LUNG RESUSCITATOR	DRM	1976-12-09	View
510(k)	K760017	CONSIOUS SEDATION (ANALOR P-76)	BZR	1976-07-20	View

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