510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
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K862436Substantially Equivalent

Trans- Circothyrotomy Device (Acc. Ravussin)

Acutronic Medical Systems AG, Jona-Rapper Swril, CH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K862436 is the FDA 510(k) clearance record for TRANS- CIRCOTHYROTOMY DEVICE (ACC. RAVUSSIN), a class II device, cleared for Acutronic Medical Systems AG on under FDA product code BTO (Tube, Tracheostomy (W/Wo Connector)). FDA records list 12 510(k) clearances for Acutronic Medical Systems AG, from to . As of , FDA records show no recalls naming K862436.

Clearance record

Decision date
Received
(130 days to decision)
Product code
BTO Tube, Tracheostomy (W/Wo Connector)
Regulation
21 CFR 868.5800
Device class
Class II
Review panel
Anesthesiology
Applicant
Acutronic Medical Systems AG Kreuzstrasse 100, Jona-Rapper Swril, CH
Third party review
No

Clearances, product code BTO

Trailing 12 months
1 clearance under product code BTO in the twelve months to October 2026, September 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code BTO, 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 20261
October 20260