510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K210992Substantially Equivalent

Altech® Exhalation Valve (Single Limb and Dual Limb)

Meditera Tibbi Malzeme San ve Tic AS, Tire Izmir, TR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K210992 is the FDA 510(k) clearance record for Altech® Exhalation Valve (Single Limb and Dual Limb), a class II device, cleared for Meditera Tibbi Malzeme San VE Tic AS on under FDA product code CBP (Valve, Non-Rebreathing). FDA records list 3 510(k) clearances for Meditera Tibbi Malzeme San VE Tic AS, from to . As of , FDA records show no recalls naming K210992.

Clearance record

Decision date
Received
(265 days to decision)
Product code
CBP Valve, Non-Rebreathing
Regulation
21 CFR 868.5870
Device class
Class II
Review panel
Anesthesiology
Applicant
Meditera Tibbi Malzeme San VE Tic AS Ibni Melek Osb Mah, Toshi Yol 4 Sol. # 29 Tire, Tire Izmir, TR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code CBP

Trailing 12 months

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

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