Jms North America Corp.
Jms North America Corp. holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2010.
Top product codes for Jms North America Corp.
Recent clearances by Jms North America Corp.
- K093637 — JMS BLUNT A. V. FISTULA NEEDLE SET WITH SITE PREPARATION TOOL MODEL 820-5300, 820-6300 AND 820-7300
- K082882 — A.V. FISTULA BLUNT NEEDLE SET
- K070234 — JMS SYSLOC MINI AVF AND APHERESIS NEEDLE SETS
- K070143 — JMS PLANECTA STOPCOCK
- K051814 — JMS SYSLOC MINI A.V. FISTULA NEEDLE SET AND APHERESIS NEEDLE SET
- K032975 — JMS BLOOD TUBING SETS
- K032977 — JMS BYPASS TUBE
- K040247 — PLUME SAFETY AVF NEEDLE
- K030479 — JMS SYSLOC A.V. FISTULA NEEDLE SET, JMS SYSLOC APHERESIS NEEDLE SET
- K023668 — JMS EXTENSION SET WITH PLANECTA, PLANECTA (STAND ALONE UNIT), PLANECTA LOCK & PLANECTA ADAPTOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.