Company · US

Medway

FDA 510(k) clearances and medical device recalls filed under this name, 1991 to 1994. 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
KMI	Monitor, Bed Patient	2
BYG	Mask, Oxygen	1
FOZ	Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days	1
KMK	Device, Intravascular Catheter Securement	1

Decided	510(k)	Device and applicant	Code
Apr 29, 1994	K934344	HOME AMB-ALERT Medway	KMI
Aug 20, 1993	K931952	MEDWAY OXYGEN MASK Medway	BYG
Oct 28, 1991	K911251	FLEX-IV Medway	FOZ
Sep 13, 1991	K911079	AMB-ALERT Medway	KMI
Jun 6, 1991	K910880	COMFOR-BOARD Medway	KMK

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