The following data is part of a premarket notification filed by Karl Storz Endoscopy-america, Inc. with the FDA for Modification To Ksea Endotip System.
| Device ID | K011359 |
| 510k Number | K011359 |
| Device Name: | MODIFICATION TO KSEA ENDOTIP SYSTEM |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | KARL STORZ ENDOSCOPY-AMERICA, INC. 600 CORPORATE POINTE Culver City, CA 90230 -7600 |
| Contact | James A Lee |
| Correspondent | James A Lee KARL STORZ ENDOSCOPY-AMERICA, INC. 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 | 2001-05-03 |
| Decision Date | 2001-06-28 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04048551235072 | K011359 | 000 |
| 04048551235034 | K011359 | 000 |