FDA.report

510(k) K022257

Device
VOMED PERIPHERAL VASCULAR ACCESSORIES, MODELS 1010 XXX-7090 XXX & 9006 XXX-9011 XXX
Applicant
Vomed Volzer Medizintechnik GmbH & Co.
510(k) number
K022257
Product code
DRC
Decision
Substantially Equivalent (SESE)
Decision date
2002-10-04
Date received
2002-07-12
Regulation
870.1390
Classification name
Trocar
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
DAGMAR MASER
Address
Amstel 320-I Amsterdam, Nh NL 1017AP 1017AP

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF not indicated by FDA · openFDA JSON

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