The following data is part of a premarket notification filed by Disetronic Medical Systems with the FDA for Disetronic Multifuse Infusion Pump System.
Device ID | K990259 |
510k Number | K990259 |
Device Name: | DISETRONIC MULTIFUSE INFUSION PUMP SYSTEM |
Classification | Pump, Infusion |
Applicant | DISETRONIC MEDICAL SYSTEMS 7690 CAMERON CIRCLE Ft. Meyers, FL 33912 |
Contact | Lee Leichter |
Correspondent | Lee Leichter DISETRONIC MEDICAL SYSTEMS 7690 CAMERON CIRCLE Ft. Meyers, FL 33912 |
Product Code | FRN |
CFR Regulation Number | 880.5725 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-01-27 |
Decision Date | 1999-02-12 |
Summary: | summary |