The following data is part of a premarket notification filed by Karl Storz Endoscopy-america, Inc. with the FDA for Karl Storz Adapters For Documentation Purposes.
| Device ID | K950336 |
| 510k Number | K950336 |
| Device Name: | KARL STORZ ADAPTERS FOR DOCUMENTATION PURPOSES |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | KARL STORZ ENDOSCOPY-AMERICA, INC. 600 CORPORATE POINTE Culver City, CA 90230 -7600 |
| Contact | Betty M Johnson |
| Correspondent | Betty M Johnson 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 | 1995-01-27 |
| Decision Date | 1995-02-13 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04048551174081 | K950336 | 000 |
| 04048551116692 | K950336 | 000 |
| 04048551116685 | K950336 | 000 |
| 04048551116661 | K950336 | 000 |