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

MEDICULT VITRIFICATION COOLING/WARMING, MODEL REF: 1228, 1229

K Number: K100367 · Decision Aug 27, 2010
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
258
Applicant Total
14
Review Days
196

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Basic Information

Device Name
MEDICULT VITRIFICATION COOLING/WARMING, MODEL REF: 1228, 1229
K Number
K100367
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.6180
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Origio A/S
Date Received
February 12, 2010
Decision Date
August 27, 2010
Product Code
MQL
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
MQL Media, Reproductive

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Other Clearances by Origio A/S

K Number Device Name
K200815 VitriGuard
K180740 VitriGuard
K173624 ORIGIO® Handling™ without phenol red (Cat. No. 8310), ORIGIO® Handling™ with phenol red (Cat. No. 8311)
K172197 SAGE 1-Step GM-CSF with HSA, SAGE 1-Step GM-CSF with SPS
K161547 Transem and EchoGen Embryo Transfer Catheters
K162833 VitriGuard
K153267 ORIGIO Gradient 100, ORIGIO Gradient 90, ORIGIO Gradient 40/80, ORIGIO Sperm Wash
K152932 BlastGen
K140317 EMBRYOGEN
K133912 ORIGIO SEQUENTIAL FERT, ORIGIO SEQUENTIAL FERT WITH PHENOL RED, ORIGIO SEQUENTIAL CLEAV, ORIGIO SEQUENTIAL CLEAV, ORIGIO
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