Aspen Laboratories, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 55
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K981220 | SYSTEM 7500 ABC ELECTROSURGICAL UNIT | April 21, 1998 |
| K963088 | SHEATH, ELECTROSURGICAL PENCIL | September 13, 1996 |
| K955834 | SYSTEM 6500 ABC ELECTROSURGICAL UNIT | July 11, 1996 |
| K960296 | 4000 ETM | February 20, 1996 |
| K953081 | BEAMER PLUS | October 30, 1995 |
| K953007 | EXCALIBUR PLUS ELECTROSURGICAL UNIT | August 21, 1995 |
| K946104 | SMOKIEVAC ELECTROSURGICAL PENCIL | April 3, 1995 |
| K944012 | ELECTROSURGICAL FLEXIBLE ELECTRODE IN-LINE SUCTION COAGULATOR | December 21, 1994 |
| K924960 | EXCALIBUR ELECTROSURGICAL UNIT | April 16, 1993 |
| K913213 | SINGLE USE LEE ELECTRODE | February 13, 1992 |
| K896838 | BISTAT ELECTROSURGICAL UNIT 60-5400-001 | February 13, 1990 |
| K896839 | MF-450 ELECTROSURGICAL UNIT 60-5500-001 | February 2, 1990 |
| K872868 | ASPEN ESMARK BANDAGE | July 31, 1987 |
| K872661 | RGB CAMERA SYSTEM | July 21, 1987 |
| K871648 | TMJ CANNULA SET | June 8, 1987 |
| K870784 | A.T.S. 1500 TOURNIQUET | March 18, 1987 |
| K863590 | UNIVERSAL CANNULA SYSTEM | October 23, 1986 |
| K862564 | A.C.L. GUIDE KIT | August 18, 1986 |
| K854751 | ZIMMER VIDEO PRODUCTS AUTOMATIC LIGHT SOURCE | February 28, 1986 |
| K860463 | SINGLE AND DUAL TOURNIQUET CUFF | February 25, 1986 |