Wieland Edelmetalle GmbH & Co.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 14
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K020347 | AGC SPEZIALLEGIERUNG | April 24, 2002 |
| K012839 | AUROPAL, ORDER-NO.: 2101 | December 31, 2001 |
| K012841 | DUO PAL 6, ORDER-NO.: 2154 | November 20, 2001 |
| K012843 | PORTADUR P 2, MODEL #2031 | November 2, 2001 |
| K012828 | PORTA SMK 82, MODEL 2032 | November 1, 2001 |
| K012835 | PORTA MAXIMUM, MODEL# 2066 | November 1, 2001 |
| K012834 | PORTA GEO TI MODEL #2004 | November 1, 2001 |
| K012826 | BIOPORTA G, MODEL 2052 | November 1, 2001 |
| K012831 | BIO PORTADUR, ORDER-NO.:2017 | November 1, 2001 |
| K012827 | PORTA AURIUM, MODEL 2067 | November 1, 2001 |
| K012838 | ERO50, ORDER-NO.: 2070 | October 23, 2001 |
| K012840 | EURO 45, ORDER-NO.: 2064 | October 23, 2001 |
| K012156 | IMAGINE H.E. | August 16, 2001 |
| K001041 | AGC-GOLD ELECTROLYTE FOR AGC-MICRO, AGC-GOLD ELECTROLYTE FOR AGC-SPEED, AGC-GOLDBONDER, AGC GLAVANOG | May 23, 2000 |