The following data is part of a premarket notification filed by Stryker Endoscopy with the FDA for Merdoc System.
| Device ID | K022393 |
| 510k Number | K022393 |
| Device Name: | MERDOC SYSTEM |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | Stryker Endoscopy 5900 OPTICAL CT. San Jose, CA 95138 |
| Contact | Kiran Javadekar |
| Correspondent | Kiran Javadekar Stryker Endoscopy 5900 OPTICAL CT. San Jose, CA 95138 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-07-23 |
| Decision Date | 2003-06-05 |
| Summary: | summary |