The following data is part of a premarket notification filed by Gyrus Acmi, Inc. with the FDA for Gyrus Acmi Cyber Wand-sterilization Trays Model Fgt.
| Device ID | K102970 |
| 510k Number | K102970 |
| Device Name: | GYRUS ACMI CYBER WAND-STERILIZATION TRAYS MODEL FGT |
| Classification | Sterilization Wrap Containers, Trays, Cassettes & Other Accessories |
| Applicant | GYRUS ACMI, INC. 136 TURNPIKE RD. Southborough, MA 01772 |
| Contact | Lorraine Calzetta |
| Correspondent | Lorraine Calzetta GYRUS ACMI, INC. 136 TURNPIKE RD. Southborough, MA 01772 |
| Product Code | KCT |
| CFR Regulation Number | 880.6850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-10-06 |
| Decision Date | 2011-05-20 |
| Summary: | summary |