Company · US

Ihara Medics U.S., Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1990 to 1996. 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
JIN	Nitroprusside, Ketones (Urinary, Non-Quant.)	4
JMK	Acid, Alpha-Ketobutyric And Nadh (U.V.), Hydroxybutyric Dehydrogenase	1

Decided	510(k)	Device and applicant	Code
May 2, 1996	K953452	KETOREX C SANWA Ihara Medics U.S., Inc.	JMK
Jul 1, 1991	K912373	KETO-340 II Ihara Medics U.S., Inc.	JIN
Dec 20, 1990	K903365	KETOREX SANWA STANDARDS Ihara Medics U.S., Inc.	JIN
Nov 20, 1990	K903367	KETONE TEST A SANWA STANDARD Ihara Medics U.S., Inc.	JIN
Nov 20, 1990	K903366	KETONE TEST B SANWA STANDARD Ihara Medics U.S., Inc.	JIN

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