Continental Medical Laboratories, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K964827 | PROD. NO. 01-132 - SUTURE REMOVAL KIT | February 14, 1997 |
| K963234 | STAPLE REMOVAL KIT | October 21, 1996 |
| K963443 | PROD. NO. 02-031 - LACERATION TRAY | October 17, 1996 |
| K962078 | TRACHEOSTOMY CLEANING TRAY W/SUCTION CATHETER | October 11, 1996 |
| K954728 | PROD NO. 01-1694 - 4X4 FOAM DRESSING | September 23, 1996 |
| K962073 | URETHRAL CATHETERIZATION TRAY/UNIVERSAL URETHRAL CATH TRAY | June 21, 1996 |
| K952335 | WOUND CARE MANAGEMENT KITS | June 14, 1995 |
| K905123 | G-TUBE DRESSING CHANGE TRAY | March 27, 1991 |