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

Accuvue+

K Number: K201058 · Decision May 6, 2020
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
422
Applicant Total
6
Review Days
15

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Basic Information

Device Name
Accuvue+
K Number
K201058
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Radmedix, LLC
Date Received
April 21, 2020
Decision Date
May 6, 2020
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 Radmedix, LLC

K Number Device Name
K231995 AcuityUDR
K231709 AcuityDR 1013 G4, AcuityDR 1417 G4, AcuityDR 1717G4
K210919 AcuityDRe
K200726 AcuityPDR
K193360 Acuity SDR Standard, Acuity SDR Plus, Acuity FDR Standard