The following data is part of a premarket notification filed by Codman & Shurtleff, Inc. with the FDA for Codman Sterilization Containers.
| Device ID | K092437 |
| 510k Number | K092437 |
| Device Name: | CODMAN STERILIZATION CONTAINERS |
| Classification | Sterilization Wrap Containers, Trays, Cassettes & Other Accessories |
| Applicant | Codman & Shurtleff, Inc. 325 PARAMOUNT DR. Raynham, MA 02767 -0350 |
| Contact | Paul Amaral |
| Correspondent | Paul Amaral Codman & Shurtleff, Inc. 325 PARAMOUNT DR. Raynham, MA 02767 -0350 |
| Product Code | KCT |
| CFR Regulation Number | 880.6850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-08-07 |
| Decision Date | 2010-03-25 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00887482141472 | K092437 | 000 |
| 00887482141458 | K092437 | 000 |
| 00887482141434 | K092437 | 000 |
| 00887482140918 | K092437 | 000 |
| 00887482128411 | K092437 | 000 |
| 00887482073896 | K092437 | 000 |
| 00887482059159 | K092437 | 000 |