The following data is part of a premarket notification filed by Harleco with the FDA for Gemsaec Appli. For Ultrazyme Plus Alp*.
Device ID | K772033 |
510k Number | K772033 |
Device Name: | GEMSAEC APPLI. FOR ULTRAZYME PLUS ALP* |
Classification | Acid, Alpha-ketobutyric And Nadh (u.v.), Hydroxybutyric Dehydrogenase |
Applicant | HARLECO 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | JMK |
CFR Regulation Number | 862.1380 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1977-10-27 |
Decision Date | 1977-11-17 |