The following data is part of a premarket notification filed by Currie Medical Specialties, Inc. with the FDA for Ck10000 Series Pouch & Bags Etc..
| Device ID | K834558 |
| 510k Number | K834558 |
| Device Name: | CK10000 SERIES POUCH & BAGS ETC. |
| Classification | Sterilization Wrap Containers, Trays, Cassettes & Other Accessories |
| Applicant | CURRIE MEDICAL SPECIALTIES, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | KCT |
| CFR Regulation Number | 880.6850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-12-28 |
| Decision Date | 1984-09-05 |