Arrow Intl., Inc.
Arrow Intl., Inc. holds FDA 510(k) medical device clearances, first cleared 1976, most recent 2010.
Clearances by Arrow Intl., Inc. — page 2
101–110 of 110- K801912 — ARROW POSITIVE PLACEMENT CON/EPIDURAL AN
- K781469 — POSITIVE PLACEMENT ANETHESIA KIT
- K781846 — ADAPTER, CATHETER SHEATH
- K781978 — PUNCTURE KIT, DISPOSALBE VEIN
- K780532 — PERCUTANEOUS SHEATH INTRODUCER KIT
- K770461 — ANESTHESIA KIT, EPIDURAL BLOCK, CONTINU.
- K770462 — PUNCTURE KIT, INTERNAL JUGULAR
- K770356 — ANESTHESIA KIT, EPIDURAL, SINGLE SHOT
- K761098 — FILTER DEVICES
- K761162 — BRACHIAL PLEXUS BLOCK ANESTHESIA KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.