510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K151485Substantially Equivalent

Genesis

Dornier Medtech America, Inc., Kennesaw GA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K151485 is the FDA 510(k) clearance record for GENESIS, a class II device, cleared for Dornier Medtech America, Inc. on under FDA product code JAA (System, X-Ray, Fluoroscopic, Image-Intensified). FDA records list 46 510(k) clearances for Dornier Medtech America, Inc., from to . As of , FDA records show no recalls naming K151485.

Clearance record

Decision date
Received
(28 days to decision)
Product code
JAA System, X-Ray, Fluoroscopic, Image-Intensified
Regulation
21 CFR 892.1650
Device class
Class II
Review panel
Radiology
Applicant
Dornier Medtech America, Inc. 1155 Roberts Blvd., Kennesaw GA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JAA

Trailing 12 months
1 clearance under product code JAA in the twelve months to October 2026, May 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JAA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260