510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K051418Substantially Equivalent

Direct Digitizer Regius Model 370

Konica Minolta Medical & Graphic, Inc., Mie-Ken, JP / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K051418 is the FDA 510(k) clearance record for DIRECT DIGITIZER REGIUS MODEL 370, a class II device, cleared for Konica Minolta Medical & Graphic, Inc. on under FDA product code MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager)). FDA records list 27 510(k) clearances for Konica Minolta Medical & Graphic, Inc., from to . As of , FDA records show one recall naming K051418.

Clearance record

Decision date
Received
(30 days to decision)
Product code
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)
Regulation
21 CFR 892.1680
Device class
Class II
Review panel
Radiology
Applicant
Konica Minolta Medical & Graphic, Inc. 319 Akeno, Mie-Ken, JP
510(k) summary
Statement
Third party review
No

Clearances, product code MQB

Trailing 12 months
3 clearances under product code MQB in the twelve months to October 2026, June 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code MQB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20262
July 20261
August 20260
September 20260
October 20260