The following data is part of a premarket notification filed by Amici, Inc. with the FDA for Amici Krypton Administration System, Modification.
Device ID | K904684 |
510k Number | K904684 |
Device Name: | AMICI KRYPTON ADMINISTRATION SYSTEM, MODIFICATION |
Classification | System, Rebreathing, Radionuclide |
Applicant | AMICI, INC. 518 VINCENT ST. Spring City, PA 19475 |
Contact | Michael Bono |
Correspondent | Michael Bono AMICI, INC. 518 VINCENT ST. Spring City, PA 19475 |
Product Code | IYT |
CFR Regulation Number | 892.1390 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-08-15 |
Decision Date | 1991-01-14 |