Company · US

Mckesson Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1976 to 1977. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
BTM	Ventilator, Emergency, Manual (Resuscitator)	1
BZR	Mixer, Breathing Gases, Anesthesia Inhalation	1
CAO	Airway, Esophageal (Obturator)	1
CBN	Apparatus, Gas-Scavenging	1
DRM	Compressor, Cardiac, External	1

Decided	510(k)	Device and applicant	Code
Aug 2, 1977	K771175	RESUSCITATOR, MS30 Mckesson Corp.	BTM
Dec 13, 1976	K761196	NITROUS OXIDE SCAVENGING MASK Mckesson Corp.	CBN
Dec 9, 1976	K761195	ESOPHAGEAL OBTURATION AIRWAY Mckesson Corp.	CAO
Dec 9, 1976	K761194	HLR QUICK-FIT HEART-LUNG RESUSCITATOR Mckesson Corp.	DRM
Jul 20, 1976	K760017	CONSIOUS SEDATION (ANALOR P-76) Mckesson Corp.	BZR

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.