FDA.report

510(k) K896907

Device
3m Iv Flow Regulator
Applicant
3M COMPANY
510(k) number
K896907
Product code
LDR
Decision
Substantially Equivalent (SESE)
Decision date
1990-02-26
Date received
1989-12-08
Regulation
880.5725
Classification name
Controller, Infusion, Intravascular, Electronic
Medical specialty
General Hospital
Review panel
General Hospital
Device class
2
Clearance type
Traditional
Third party reviewed
No

Related Records

Applicant Contact

Contact
VON BUSCH
Address
1120 Red Fox Rd. St. Paul MN US 55112 55112

FDA Registration Numbers

Source Documents

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code LDR

510(k)DeviceApplicantDecision date
K242693DEKA Infusion System, DEKA Administration SetDeka Research and Development Corporation2024-10-07
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K153760Volumetric Infusion ControllerDEKA Research & Development2016-10-03
K963136PACER MODEL 100 INFUSION CONTROLLERHealth Watch, Inc.1997-10-10
K971865ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500-3PAlexander Mfg. Co.1997-07-03
K971826ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER M12/500Alexander Mfg. Co.1997-07-03
K934543UNIVERSAL CONTROLLER, MODEL 100Metamed, Inc.1994-03-29
K935236FLOW CONTROLLING EXTENSION SETBlock Medical, Inc.1994-02-24
K905498STAT 2 IV PUMPETTEThe Master Medical Corp.1991-04-16
K905497MASTER FLOW I.V. PUMPETTEThe Master Medical Corp.1991-04-16
K894111VARI-SETSonex Medical1989-09-28
K894487IVAC(R) VOLUMETRIC CONTROLLER - MODEL 262+Y1989-09-27
K893487LIFECARE 75 CONTROLLERAbbott Laboratories1989-07-28
K884307IVAC(R) VOLUMETRIC CONTROLLER - MODEL 262Y1988-11-01
K882167IVY COMMANDER, MODEL 600Ivy Medical, Inc.1988-09-23