FDA 510(k) FDA class 2 Substantially Equivalent - Subject to Tracking Reg. 🇺🇸 United States

DISPOSABLE, AMBULATORY, INFUSION PUMPS

K Number: K940406 · Decision Sep 2, 1994
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
87
Applicant Total
12
Review Days
218

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Basic Information

Device Name
DISPOSABLE, AMBULATORY, INFUSION PUMPS
K Number
K940406
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent - Subject to Tracking Reg.
Applicant
Vlv Associates, Inc.
Date Received
January 27, 1994
Decision Date
September 2, 1994
Product Code
MEB
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MEB Pump, Infusion, Elastomeric

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Other Clearances by Vlv Associates, Inc.

K Number Device Name
K972957 SA-EF MULTI-LUMEN EXTENSION SET
K964876 SA.EF(TM) INFUSION PORT II - CONNECTOR AND EXTENSION SET
K955783 VLV SA.EF INFUSION PORT EXTENSION SETS
K953791 VLV SA EF INFUSION PORT
K945592 VLV SOLODRAW(TM) DUAL CHAMBER PISTON SYRINGE
K933364 PROMED BIOPSY NEEDLE
K922469 PRO-LOK EXTENSION SET(S)
K904217 PRO-LOK (TM) EXTENSION SETS
K901046 VERSA-LOCK(TM) UNIVERSAL NEEDLE CONNECTOR
K901081 PRO-LOCK(TM) SHIELDING NEEDLE CONNECTOR ASSEMBLY
Search all 12 clearances from Vlv Associates, Inc. →