510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K073104Substantially Equivalent

Skintact and Various Other Tradenames

Leonhard Lang GmbH, Stillwater MN / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K073104 is the FDA 510(k) clearance record for SKINTACT AND VARIOUS OTHER TRADENAMES, a class II device, cleared for Leonhard Lang GmbH on under FDA product code DRX (Electrode, Electrocardiograph). FDA records list 19 510(k) clearances for Leonhard Lang GmbH, from to . As of , FDA records show no recalls naming K073104.

Clearance record

Decision date
Received
(14 days to decision)
Product code
DRX Electrode, Electrocardiograph
Regulation
21 CFR 870.2360
Device class
Class II
Review panel
Cardiovascular
Applicant
Leonhard Lang GmbH P.O. Box 560, Stillwater MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DRX

Trailing 12 months

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

FDA records show no clearances under product code DRX in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DRX, 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