The following data is part of a premarket notification filed by Medfusion Systems, Inc. with the FDA for Ambulatory Infusion Pump Drug Reservoir.
Device ID | K870524 |
510k Number | K870524 |
Device Name: | AMBULATORY INFUSION PUMP DRUG RESERVOIR |
Classification | Pump, Infusion |
Applicant | MEDFUSION SYSTEMS, INC. 3070 BUSINESS PARK DR. Norcross, GA 30071 |
Contact | Ruffin Booth |
Correspondent | Ruffin Booth MEDFUSION SYSTEMS, INC. 3070 BUSINESS PARK DR. Norcross, GA 30071 |
Product Code | FRN |
CFR Regulation Number | 880.5725 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-02-06 |
Decision Date | 1987-05-06 |