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

TUBALGATOR

K Number: K113080 · Decision Jun 29, 2012
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
15
Applicant Total
9
Review Days
255

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Basic Information

Device Name
TUBALGATOR
K Number
K113080
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4150
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Mectra Labs, Inc.
Date Received
October 18, 2011
Decision Date
June 29, 2012
Product Code
HIN
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
HIN Coagulator-Cutter, Endoscopic, Bipolar (And Accessories)

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K934547 MECTRA TROCAR
K935382 GRASPERS
K925691 INSUFFLATION TUBING
K920959 INSUFFLATOR, LAPAROSCOPIC