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

INSUFLOW SYNERGY PORT

K Number: K120640 · Decision Jul 18, 2012
Classifications
1
FEI Numbers
141
Registration Numbers
141
Same Product Code
176
Applicant Total
13
Review Days
138

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Basic Information

Device Name
INSUFLOW SYNERGY PORT
K Number
K120640
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1730
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Lexion Medical, LLC
Date Received
March 2, 2012
Decision Date
July 18, 2012
Product Code
HIF
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
HIF Insufflator, Laparoscopic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HIF), ordered by most recent decision date.

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Other Clearances by Lexion Medical, LLC

K Number Device Name
K191780 AP50/30 Insufflator with Insuflow Port
K170799 AP 50/30 Insufflator with Insuflow Port
K140263 INSUFLOW SYNERGY PORT, INSUFLOW SYNERGY XL PORT
K132203 PNEUVIEW XE VERYCLEAR GAS EVACUATION CANNULA
K132204 INSUFLOW SYNERGY XL PORT
K112357 VESSEL GUARDIAN
K102136 VESSEL GUARDIAN
K101320 VASOVAPOR
K091366 INSUFLOW DEWHEART
K090456 INSUFLOW
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