LAPAROCAM
Laparoscope, General & Plastic Surgery
KARL STORZ ENDOSCOPY
The following data is part of a premarket notification filed by Karl Storz Endoscopy with the FDA for Laparocam.
Pre-market Notification Details
| Device ID | K992541 |
| 510k Number | K992541 |
| Device Name: | LAPAROCAM |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | KARL STORZ ENDOSCOPY 600 CORPORATE POINTE Culver City, CA 90230 -7600 |
| Contact | Kevin Kennan |
| Correspondent | Kevin Kennan KARL STORZ ENDOSCOPY 600 CORPORATE POINTE Culver City, CA 90230 -7600 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-07-30 |
| Decision Date | 1999-08-19 |
| Summary: | summary |
Trademark Results [LAPAROCAM]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 LAPAROCAM 74301490 1799236 Dead/Cancelled |
KARL STORZ GMBH & CO. KG 1992-08-06 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.