FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

DISPENSER DP 20

K Number: K071588 · Decision Nov 26, 2007
Classifications
1
FEI Numbers
149
Registration Numbers
149
Same Product Code
847
Applicant Total
11
Review Days
168

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Basic Information

Device Name
DISPENSER DP 20
K Number
K071588
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
NOUVAG AG
Date Received
June 11, 2007
Decision Date
November 26, 2007
Product Code
FRN
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
FRN Pump, Infusion

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Other Clearances by NOUVAG AG

K Number Device Name
K080365 MORCE POWER PLUS AND VARIOCARVE MORCELLATOR
K081191 TCM ENDO 20
K042822 TCM ENDO V, MODEL 1534
K042943 NOUVAG AG - VACUSON 40 AND VACUSON 60
K042434 MICRO-MOTORSYSTEMS MD20, SEM2, HIGHSURG 20 & DT55
K022505 CONTRA-ANGLE, MODELS 1059, 5050, 5051, 5055, 5056, 5057, 5059, 5060, 5061, 5062, 5063, 5064, 5065, 5066, 5067, 5068,
K013185 TCM ENDO III
K000710 MD 10, SEM, SM 12, CBM
K981679 TCM 3000 AND TCM ENDO
K954722 MICRO-DISPENSER 7000 & MICRODISPENSER 8000
Search all 11 clearances from NOUVAG AG →