Nipro Medical Corp.
Nipro Medical Corp. appears in FDA public data with 0 recalls, 27 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Jan 22, 2010.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 27
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K093985 | NIPRO SAFETOUCH LOCKTAIL SAFETY FISTULA NEEDLE | Jan 22, 2010 |
| K081210 | NIPRO SAFETOUCH HUBER INFUSTION SET | Oct 21, 2008 |
| K072024 | NIPRO BLOOD TUBING SET WITH TRANSDUCER PROTECTOR AND PRIMING SET, MODEL A201-A219, V801-V806, 5M9634 | Oct 4, 2007 |
| K063368 | NIPRO BIOHOLE NEEDLE | Feb 5, 2007 |
| K063721 | NIPRO SAFETOUCH II GAMMA | Jan 12, 2007 |
| K052474 | NIPRO HYPODERMIC NEEDLE | Nov 10, 2005 |
| K051574 | NIPRO DISPOSABLE SYRINGE WITH OR WITHOUT NEEDLE | Aug 26, 2005 |
| K041779 | NIPRO DISPOSABLE STOPCOCKS, MODELS 3W-RC. NCN-3, 3W-R, 3W-L | Sep 21, 2004 |
| K032777 | MODIFICATION TO: NIPRO SAFE TOUCH SAFETY FISTULA NEEDLE | Nov 14, 2003 |
| K030683 | NIPRO DISPOSABLE SYRINGES | Oct 31, 2003 |
| K022756 | NIPRO BIO-FLEX CATHETER | Oct 18, 2002 |
| K013293 | NIPRO HYPODERMIC NEEDLE | Dec 14, 2001 |
| K013287 | NIPRO SAFELET CATH | Dec 3, 2001 |
| K011297 | NIPRO SAFETOUCH SCALP VEIN AND BLOOD COLLECTION SET | Jun 20, 2001 |
| K010264 | NIPRO BLOOD TUBING SET FOR HEMODIALYSIS WITH TRANSDUCER PROTECTORS AND PRIMING SET | Apr 27, 2001 |
| K003394 | APPALEAD GW+03XXXXXXR SERIES | Jan 30, 2001 |
| K001465 | NIPRO BLOOD TUBING SET FOR HEMODIALYSIS WITH TRANSDUCER PROTECTORS AND PRIMING SET | Dec 5, 2000 |
| K002813 | NIPRO SAFETOUCH SAFETY FISTULA NEEDLE | Nov 21, 2000 |
| K001251 | SNIPER, MODEL OR-3872XX SERIES | Jul 7, 2000 |
| K992699 | NIPRO BLOOD COLLECTION NEEDLE | Feb 14, 2000 |