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

GEL MARK V

K Number: K050090 · Decision Feb 7, 2005
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
109
Applicant Total
30
Review Days
24

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Basic Information

Device Name
GEL MARK V
K Number
K050090
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Senorx, Inc.
Date Received
January 14, 2005
Decision Date
February 7, 2005
Product Code
NEU
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
NEU Marker, Radiographic, Implantable

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Other Clearances by Senorx, Inc.

K Number Device Name
K233220 EnCor Enspire™Breast Biopsy System (E4115, E4230); EnCor™ Breast Biopsy Driver (DRENCOR); EnCor™ MRI Breast Biopsy Driver (DRENCORMR); EnCor™ Breast Biopsy Driver Probes (ECP017G, ECP017GV, ECP0110G, ECP0110GV, ECP0112G, ECP0112GV); EnCor™ MRI Breast Biopsy Probes (ECPMR017G, ECPMR0110G, ECPMR0110GBT)
K210654 EnCor Breast Biopsy Probe with Rinse Tube
K161805 EnCor MRI Introducer Set, EnCor Probe Introducer
K131654 STARCHMARK BREAST TISSUE MARKER; STARCHMARK ULTRACOR BREAST TISSUE MARKER
K093512 ENCOR BREAST BIOPSY SYSTEM
K092323 CONTURA CAVITY MAINTENANCE CATHETER
K082264 CONTURA LUMEN MARKER
K081085 STARCHMARK BIOPSY SITE MARKER, MODEL STMKEC-10GSS, STMKEC-10GTR, STMKMT-11GS
K081170 PROSTATE TISSUE MARKER
K081079 CONTURA MLB SOURCE APPLICATOR FOR BRACHYTHERAPY
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