510(k) K910323

Device
Bedside Fluid Management System 1000 (fms-1000)
Applicant
UAB RESEARCH FOUNDATION
510(k) number
K910323
Product code
FLN
Decision
Substantially Equivalent (SESE)
Decision date
1991-10-03
Date received
1991-01-24
Regulation
880.2420
Classification name
Monitor, Electric For Gravity Flow Infusion Systems
Medical specialty
General Hospital
Review panel
General Hospital
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
KENNETH J ROOZEN
Address
P.O. Box 1000 Uab Station Birmingham AL US 35294 35294

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code FLN#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K172242DripAssist PlusShift Labs, Inc.2018-05-25
K150687DripAssistShift Labs2015-10-13
K133870FLUID LEVEL MONITORColeman Laboratories2014-04-24
K080704LOW FLUID ALARMEm-Tec GmbH2008-04-17
K050783ISSYS DRUG FLOW MONITORIntegrated Sensing Systems, Inc.2006-02-22
K060123LEVELERT II FLUID LEVEL SENSORSmith & Nephew, Inc.2006-02-14
K030136DRIP ALERTDrip Alert, Inc.2003-04-07
K022248STRYKER L3 HYDROLERTStryker Endoscopy2002-08-06
K013121MT ALERT INFUSION MONITORSierra Biosearch, Inc.2001-10-15
K973025FLUID CENTURION (4-100-00)Northgate Technologies, Inc.1997-11-20
K972084ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M212Alexander Mfg. Co.1997-07-03
K923561AC-901 I.V. INFUSION DROP COUNTERLamtic, Inc.1993-05-26
K902808DRIPTROLTrans-Pacific Healthcare-USA1990-10-01
K903193SMITH & NEPHEW DYONICS LEVELERT SYSTEMSmith & Nephew Dyonics, Inc.1990-08-30
K893693H.U. I.V. DROP COUNTERLi-Lien Corp.1989-10-27