The following data is part of a premarket notification filed by Conmed Corp. with the FDA for Conmed/aspen Labs Coated Laparoscopic Electrosurgical Blades.
| Device ID | K952204 |
| 510k Number | K952204 |
| Device Name: | CONMED/ASPEN LABS COATED LAPAROSCOPIC ELECTROSURGICAL BLADES |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | CONMED CORP. P.O. BOX 1408 Dayton, OH 45401 -1408 |
| Contact | Ira D Duesler, Jr |
| Correspondent | Ira D Duesler, Jr CONMED CORP. P.O. BOX 1408 Dayton, OH 45401 -1408 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-05-10 |
| Decision Date | 1995-05-25 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20653405010835 | K952204 | 000 |
| 20653405010705 | K952204 | 000 |
| 20653405010712 | K952204 | 000 |
| 20653405010729 | K952204 | 000 |
| 20653405010736 | K952204 | 000 |
| 20653405010743 | K952204 | 000 |
| 20653405010750 | K952204 | 000 |
| 20653405010767 | K952204 | 000 |
| 20653405010774 | K952204 | 000 |
| 20653405010811 | K952204 | 000 |
| 20653405010828 | K952204 | 000 |
| 20653405010699 | K952204 | 000 |