The following data is part of a premarket notification filed by Target Therapeutics with the FDA for Target Therapeutics Sterile Products.
| Device ID | K874815 |
| 510k Number | K874815 |
| Device Name: | TARGET THERAPEUTICS STERILE PRODUCTS |
| Classification | Catheter, Intravascular, Diagnostic |
| Applicant | TARGET THERAPEUTICS 2100 SOUTH SEPULVEDA BLVD. Los Angeles, CA 90025 |
| Contact | Marie Daniels |
| Correspondent | Marie Daniels TARGET THERAPEUTICS 2100 SOUTH SEPULVEDA BLVD. Los Angeles, CA 90025 |
| Product Code | DQO |
| CFR Regulation Number | 870.1200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-11-20 |
| Decision Date | 1988-02-05 |