The following data is part of a premarket notification filed by Radiometer America, Inc. with the FDA for Calibration Verification Kit Or Cvk.
Device ID | K924802 |
510k Number | K924802 |
Device Name: | CALIBRATION VERIFICATION KIT OR CVK |
Classification | Multi-analyte Controls, All Kinds (assayed) |
Applicant | RADIOMETER AMERICA, INC. 811 SHARON DR. Westlake, OH 44145 -1598 |
Contact | Donald L Baker |
Correspondent | Donald L Baker RADIOMETER AMERICA, INC. 811 SHARON DR. Westlake, OH 44145 -1598 |
Product Code | JJY |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-09-24 |
Decision Date | 1993-03-09 |