The following data is part of a premarket notification filed by Gyrus Acmi, Inc. with the FDA for Gyrus Acmi Flexible Endoscope Storage-sterilization Trays.
Device ID | K092682 |
510k Number | K092682 |
Device Name: | GYRUS ACMI FLEXIBLE ENDOSCOPE STORAGE-STERILIZATION TRAYS |
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 | 2009-09-01 |
Decision Date | 2009-12-11 |
Summary: | summary |