Sarstedt, Inc.
FDA Regulatory Profile
Sarstedt, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 25, 2005.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K051019 | SAFETY NEEDLE | July 25, 2005 |
| K031359 | S-MONOVETTE EDTA K2-GEL | September 12, 2003 |
| K032150 | SAFETY-MULTIFLY | September 12, 2003 |
| K024237 | URINE MONOVETTE BORIC ACID | April 14, 2003 |
| K003382 | SARSTEDT NEEDLE PROTECTOR | March 30, 2001 |
| K913622 | HEMOPLUS | January 31, 1992 |