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

MobileRay Pulse SE Digital Imaging System

K Number: K191503 · Decision Sep 4, 2019
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
319
Applicant Total
5
Review Days
90

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Basic Information

Device Name
MobileRay Pulse SE Digital Imaging System
K Number
K191503
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Portavision Medical, LLC
Date Received
June 6, 2019
Decision Date
September 4, 2019
Product Code
OWB
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
OWB Interventional Fluoroscopic X-Ray System

Similar 510(k) Clearances

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

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Other Clearances by Portavision Medical, LLC

K Number Device Name
K212557 Virtual C DRF-NEO Digital Imaging System
K211191 Virtual C DRF Digital Imaging System
K133524 PVMED DDR 2430T
K083048 NEORAY DR 2520 DIGITAL IMAGING SYSTEM