FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

EVA EMPTY MIXING CONTAINER

K Number: K932640 · Decision Nov 10, 1993
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
116
Applicant Total
19
Review Days
161

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Basic Information

Device Name
EVA EMPTY MIXING CONTAINER
K Number
K932640
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5025
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Douglas Medical Products Corp.
Date Received
June 2, 1993
Decision Date
November 10, 1993
Product Code
KPE
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
KPE Container, I.V.

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Other Clearances by Douglas Medical Products Corp.

K Number Device Name
K961155 SOLO PICC/MIDLINE CATHETER KIT MODELS 71924, 71908
K954428 SOLOPICC 24 (60CM) 20GA CATHETER
K941628 40 MICRON BLOOD TRANSFUSION FILTER
K942101 4-LEAD IRRIGATION SET
K941453 CHECK VALVE SOLUTION SET
K930854 SOLUTION SET WITH .2 MICRON FILTER
K932637 SUBCUTANEOUS INFUSION SET
K931659 3 LEAD CONNECTOR
K931658 IN-LINE BURETTE SET
K932638 HUBER NEEDLE INFUSION SET
Search all 19 clearances from Douglas Medical Products Corp. →