510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K013052Substantially Equivalent

Konica Laser Imager, Drypro Model 751/752

Konica Minolta Medical & Graphic, Inc., Hachioji-Shi Tokyo, JP / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K013052 is the FDA 510(k) clearance record for KONICA LASER IMAGER, DRYPRO MODEL 751/752, a class II device, cleared for Konica Minolta Medical & Graphic, Inc. on under FDA product code LMC (Camera, Multi Format, Radiological). FDA records list 27 510(k) clearances for Konica Minolta Medical & Graphic, Inc., from to . As of , FDA records show no recalls naming K013052.

Clearance record

Decision date
Received
(127 days to decision)
Product code
LMC Camera, Multi Format, Radiological
Regulation
21 CFR 892.2040
Device class
Class II
Review panel
Radiology
Applicant
Konica Minolta Medical & Graphic, Inc. 2970 Ishikawa-Cho, Hachioji-Shi Tokyo, JP
510(k) summary
Summary
Third party review
No

Clearances, product code LMC

Trailing 12 months

FDA records hold no clearances under product code LMC in the trailing twelve months.

FDA records show no clearances under product code LMC in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LMC, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260