510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K885139Substantially Equivalent

Modified Adult Cricothyroidotomy Kit

Pertrach, Bridgeport WV / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K885139 is the FDA 510(k) clearance record for MODIFIED ADULT CRICOTHYROIDOTOMY KIT, a class II device, cleared for Pertrach on under FDA product code BTO (Tube, Tracheostomy (W/Wo Connector)). FDA records list 2 510(k) clearances for Pertrach, from to . As of , FDA records show no recalls naming K885139.

Clearance record

Decision date
Received
(161 days to decision)
Product code
BTO Tube, Tracheostomy (W/Wo Connector)
Regulation
21 CFR 868.5800
Device class
Class II
Review panel
Anesthesiology
Applicant
Pertrach Box 1158, Bridgeport WV
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