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Company · US

American Viggo

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

10510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
FMG	Stopcock, I.V. Set	4
CAZ	Anesthesia Conduction Kit	1
FMI	Needle, Hypodermic, Single Lumen	1
FOZ	Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days	1
FPA	Set, Administration, Intravascular	1
FPK	Tubing, Fluid Delivery	1
KGZ	Accessories, Catheter	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Aug 2, 1977	K771339	MALE LUER LOCK PLUG American Viggo	FPA
Apr 29, 1977	K770528	NEEDLE, MEMBRANE American Viggo	FMI
Mar 30, 1977	K770181	I.V. CATHETER PLACEMENT UNIT American Viggo	FOZ
Mar 30, 1977	K770174	LUER-LOCK EXTENSION SET American Viggo	FPK
Feb 28, 1977	K770154	3-WAY STOPCOCK WITH LUER-LOCK FITTING American Viggo	KGZ
Feb 25, 1977	K770096	EPIDURAL BLOCK PROCEDURE PACK American Viggo	CAZ
Dec 2, 1976	K760679	4-WAY STOPCOCK W/7CM TUBING, American Viggo	FMG
Dec 2, 1976	K760678	4-WAY STOPCOCK W/100 CM TUBING, LUER-LK American Viggo	FMG
Dec 2, 1976	K760667	4-WAY STOPCOCK W/10 CM EXTEN. TUBING American Viggo	FMG
Dec 2, 1976	K760666	4-WAY STOPCOCK W/LUER-LOCK FITTING American Viggo	FMG

Latest recalls

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

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