The following data is part of a premarket notification filed by Medfusion Systems, Inc. with the FDA for Volume Control Set With Extension.
Device ID | K860616 |
510k Number | K860616 |
Device Name: | VOLUME CONTROL SET WITH EXTENSION |
Classification | Set, Administration, Intravascular |
Applicant | MEDFUSION SYSTEMS, INC. 3070 BUSINESS PARK DR. Norcross, GA 30071 |
Contact | William Arthur |
Correspondent | William Arthur MEDFUSION SYSTEMS, INC. 3070 BUSINESS PARK DR. Norcross, GA 30071 |
Product Code | FPA |
CFR Regulation Number | 880.5440 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-02-19 |
Decision Date | 1986-06-02 |