510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K073162Substantially Equivalent

Safe-Cross(r) Radio Frequency Total Occlusion Crossing System, Safe-Cross(r) Radio Frequency Total Occlusion Crossing

DSM Biomedical, Inc., Exton PA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K073162 is the FDA 510(k) clearance record for SAFE-CROSS(R) RADIO FREQUENCY TOTAL OCCLUSION CROSSING SYSTEM, SAFE-CROSS(R) RADIO FREQUENCY TOTAL OCCLUSION CROSSING, a class II device, cleared for Kensey Nash Corporation on under FDA product code DQX (Wire, Guide, Catheter). FDA records list 54 510(k) clearances for DSM Biomedical, Inc., from to . As of , FDA records show no recalls naming K073162.

Clearance record

Decision date
Received
(91 days to decision)
Product code
DQX Wire, Guide, Catheter
Regulation
21 CFR 870.1330
Device class
Class II
Review panel
Cardiovascular
Applicant
Kensey Nash Corporation 735 Pennsylvania Dr., Exton PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DQX

Trailing 12 months
12 clearances under product code DQX in the twelve months to October 2026, January 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code DQX, trailing twelve months
MonthClearances
November 20251
December 20250
January 20263
February 20260
March 20263
April 20260
May 20261
June 20260
July 20262
August 20260
September 20262
October 20260