Company · US

H.W. Andersen Products, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1987 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
GBS	Catheter, Ventricular, General & Plastic Surgery	3
BSS	Tube, Nasogastric	1
FGE	Stents, Drains And Dilators For The Biliary Ducts	1

Decided	510(k)	Device and applicant	Code
Dec 30, 1994	K935688	AN-10S ANDERSEN TUBE WITH STYLET H.W. Andersen Products, Inc.	BSS
Sep 21, 1987	K872458	AN3200 DOUBILET DRAIN H.W. Andersen Products, Inc.	FGE
Jul 23, 1987	K872460	AN3000 MAHONEY DRAIN H.W. Andersen Products, Inc.	GBS
Jul 21, 1987	K872459	AN3100 MULHOLLAND DRAIN H.W. Andersen Products, Inc.	GBS
Jul 21, 1987	K872457	AN3500 WORTH DRAIN H.W. Andersen Products, Inc.	GBS

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