FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇳 India

PRORAD X-Ray Flat Panel Detector with DROC

K Number: K240771 · Decision Nov 12, 2024
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
422
Applicant Total
3
Review Days
236

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Basic Information

Device Name
PRORAD X-Ray Flat Panel Detector with DROC
K Number
K240771
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Prognosys Medical Systems Private Limited
Date Received
March 21, 2024
Decision Date
November 12, 2024
Product Code
MQB
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
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

Similar 510(k) Clearances

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

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Other Clearances by Prognosys Medical Systems Private Limited

K Number Device Name
K243473 PRORAD ATLAS ULTRAPORTABLE; PRORAD ATLAS ULTRAPORTABLE PLUS
K183541 ProRad 2FC and ProRad 3NC Stationary Radiographic Systems