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

NOUVAG AG - VACUSON 40 AND VACUSON 60

K Number: K042943 · Decision Dec 17, 2004
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
158
Applicant Total
11
Review Days
53

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Basic Information

Device Name
NOUVAG AG - VACUSON 40 AND VACUSON 60
K Number
K042943
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4780
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
NOUVAG AG
Date Received
October 25, 2004
Decision Date
December 17, 2004
Product Code
BTA
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
BTA Pump, Portable, Aspiration (Manual Or Powered)

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Other Clearances by NOUVAG AG

K Number Device Name
K080365 MORCE POWER PLUS AND VARIOCARVE MORCELLATOR
K081191 TCM ENDO 20
K071588 DISPENSER DP 20
K042822 TCM ENDO V, MODEL 1534
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 →