The following data is part of a premarket notification filed by Nor-lake, Inc. with the FDA for Refrigerator, Freezer, Blood Storage.
| Device ID | BK920020 |
| 510k Number | BK920020 |
| Device Name: | Refrigerator, Freezer, Blood Storage |
| Classification | Refrigerator, Freezer, Blood Storage |
| Applicant | Nor-Lake, Inc. second And Elm Str. P.o. Box 248 Hudson, WI 54016 |
| Product Code | KSE |
| CFR Regulation Number | 864.9700 [🔎] |
| Decision | Substantially Equivalent (SE) |
| Type | 510(k) Traditio |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-07-29 |
| Decision Date | 1993-01-19 |