The following data is part of a premarket notification filed by Pajunk Gmbh Medizintechnologie with the FDA for Veress Cannula And Modular Veress Cannula.
| Device ID | K062097 |
| 510k Number | K062097 |
| Device Name: | VERESS CANNULA AND MODULAR VERESS CANNULA |
| Classification | Laparoscope, Gynecologic (and Accessories) |
| Applicant | PAJUNK GMBH MEDIZINTECHNOLOGIE KARL-HALL-STRASSE 1 Geisingen, Baden-wurttemberg, DE 78187 |
| Contact | Christian Quass |
| Correspondent | Christian Quass PAJUNK GMBH MEDIZINTECHNOLOGIE KARL-HALL-STRASSE 1 Geisingen, Baden-wurttemberg, DE 78187 |
| Product Code | HET |
| CFR Regulation Number | 884.1720 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-07-24 |
| Decision Date | 2006-10-13 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04048223128121 | K062097 | 000 |