510(k) K043614

Device
VACULINK, MODEL VCL 3000
Applicant
Medevco, Inc.
510(k) number
K043614
Product code
HDB
Decision
Substantially Equivalent (SESE)
Decision date
2005-04-14
Date received
2004-12-30
Regulation
884.4340
Classification name
Extractor, Vacuum, Fetal
Medical specialty
Obstetrics/Gynecology
Review panel
Obstetrics/Gynecology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
KRISTA OAKES
Address
2300 Mcdermott Rd. # 200-207 Plano TX US 75025 75025

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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