Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K161534Substantially Equivalent

EasyOne Pro Respiratory Analysis System

NDD Medizintechnik AG, Zurich, CH / Traditional, Substantially Equivalent

K161534 is the FDA 510(k) clearance record for EasyOne Pro Respiratory Analysis System, a class II device, cleared for Ndd Medizintechnik AG on under FDA product code BTY (Calculator, Predicted Values, Pulmonary Function). FDA records list 4 510(k) clearances for Ndd Medizintechnik AG, from to . As of , FDA records show 2 recalls naming K161534.

Clearance record

Decision date
Received
(264 days to decision)
Product code
BTY Calculator, Predicted Values, Pulmonary Function
Regulation
21 CFR 868.1890
Device class
Class II
Review panel
Anesthesiology
Applicant
Ndd Medizintechnik AG Technoparkstrasse 1, Zurich, CH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code BTY

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