The following data is part of a premarket notification filed by Marion Laboratories, Inc. with the FDA for Droppers, Solution, Iodine.
Device ID | K781061 |
510k Number | K781061 |
Device Name: | DROPPERS, SOLUTION, IODINE |
Classification | Stains, Microbiologic |
Applicant | MARION LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JTS |
CFR Regulation Number | 864.1850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1978-06-26 |
Decision Date | 1978-08-14 |