The following data is part of a premarket notification filed by Medegen Medical Manufacturing Services with the FDA for Intravascular Administration Set And Extension Set.
Device ID | K051499 |
510k Number | K051499 |
Device Name: | INTRAVASCULAR ADMINISTRATION SET AND EXTENSION SET |
Classification | Set, Administration, Intravascular |
Applicant | MEDEGEN MEDICAL MANUFACTURING SERVICES 15 CHEROKEE Trabuco Canyon, CA 92679 |
Contact | Salvadore F Palomares |
Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
Product Code | FPA |
CFR Regulation Number | 880.5440 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2005-06-07 |
Decision Date | 2005-06-22 |
Summary: | summary |