The following data is part of a premarket notification filed by Codman & Shurtleff, Inc. with the FDA for Denver Pleuro-peritoneal Shunt.
| Device ID | K880570 |
| 510k Number | K880570 |
| Device Name: | DENVER PLEURO-PERITONEAL SHUNT |
| Classification | Shunt, Peritoneal |
| Applicant | Codman & Shurtleff, Inc. 41 PACELLA PARK DR. RANDOLPH INDUSTRIAL PARK Randolph, MA 02368 -1794 |
| Contact | G Cloutier |
| Correspondent | G Cloutier Codman & Shurtleff, Inc. 41 PACELLA PARK DR. RANDOLPH INDUSTRIAL PARK Randolph, MA 02368 -1794 |
| Product Code | KPM |
| CFR Regulation Number | 876.5955 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-02-10 |
| Decision Date | 1988-06-20 |