The following data is part of a premarket notification filed by Advance Medical Designs, Inc. with the FDA for Advance Administration Sets (varying Length).
Device ID | K900188 |
510k Number | K900188 |
Device Name: | ADVANCE ADMINISTRATION SETS (VARYING LENGTH) |
Classification | Set, Administration, Intravascular |
Applicant | ADVANCE MEDICAL DESIGNS, INC. 808 PICKENS INDUSTRIAL DR. Marietta, GA 30062 |
Contact | Ronald D Arkin |
Correspondent | Ronald D Arkin ADVANCE MEDICAL DESIGNS, INC. 808 PICKENS INDUSTRIAL DR. Marietta, GA 30062 |
Product Code | FPA |
CFR Regulation Number | 880.5440 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-01-16 |
Decision Date | 1990-05-01 |