CHEMO-PORT
Port & Catheter, Implanted, Subcutaneous, Intravascular
HDC CORP.
The following data is part of a premarket notification filed by Hdc Corp. with the FDA for Chemo-port.
Pre-market Notification Details
| Device ID | K874184 |
| 510k Number | K874184 |
| Device Name: | CHEMO-PORT |
| Classification | Port & Catheter, Implanted, Subcutaneous, Intravascular |
| Applicant | HDC CORP. 2551 CASEY AVE. Mountain View, CA 94043 |
| Contact | Carey E Bolden |
| Correspondent | Carey E Bolden HDC CORP. 2551 CASEY AVE. Mountain View, CA 94043 |
| Product Code | LJT |
| CFR Regulation Number | 880.5965 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-10-14 |
| Decision Date | 1987-12-30 |
Trademark Results [CHEMO-PORT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CHEMO-PORT 76187123 2563443 Dead/Cancelled |
HDC Corporation 2000-12-27 |
 CHEMO-PORT 73560657 1424709 Dead/Cancelled |
HDC CORPORATION 1985-09-30 |
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