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

GelPOINT V-Path Transvaginal Access Platform with Retroperitoneal Access Device

K Number: K243152 · Decision Oct 2, 2025
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
17
Applicant Total
45
Review Days
367

Basic Information

Device Name
GelPOINT V-Path Transvaginal Access Platform with Retroperitoneal Access Device
K Number
K243152
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.1640
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Applied Medical Resources Corp.
Date Received
September 30, 2024
Decision Date
October 2, 2025
Product Code
HEW
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
HEW Culdoscope (And Accessories)

Similar 510(k) Clearances

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

View all

Other Clearances by Applied Medical Resources Corp.

K Number Device Name
K252740 Voyant® Open Fusion Device (EB240/Open Fusion)
K252442 Kii Structural Balloon Access System
K201212 Voyant Open Fusion Device
K200598 Voyant Maryland Fusion Device
K193292 Voyant 5mm Fusion Device, Voyant Maryland Fusion Device
K191294 Transvaginal Access Platform
K182653 Voyant Maryland Fusion Device
K182244 Voyant Electrosurgical Generator
K182024 Dissecting Balloon System
K171701 GelPOINT Path Transanal Access Platform
Search all 45 clearances from Applied Medical Resources Corp. →