The following data is part of a premarket notification filed by Aesculap with the FDA for Aesculap Sterilcontainer System.
| Device ID | K062510 |
| 510k Number | K062510 |
| Device Name: | AESCULAP STERILCONTAINER SYSTEM |
| Classification | Wrap, Sterilization |
| Applicant | AESCULAP 3773 CORPORATE PKWY. Center Valley, PA 18034 |
| Contact | Matthew M Hull |
| Correspondent | Matthew M Hull AESCULAP 3773 CORPORATE PKWY. Center Valley, PA 18034 |
| Product Code | FRG |
| CFR Regulation Number | 880.6850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-08-28 |
| Decision Date | 2006-11-17 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00841036211295 | K062510 | 000 |
| 00841036211219 | K062510 | 000 |
| 00841036211226 | K062510 | 000 |
| 00841036211233 | K062510 | 000 |
| 00841036211240 | K062510 | 000 |
| 00841036211257 | K062510 | 000 |
| 00841036211264 | K062510 | 000 |
| 00841036211271 | K062510 | 000 |
| 00841036211288 | K062510 | 000 |
| 00841036211202 | K062510 | 000 |