510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K051889Substantially Equivalent

Carevent Ca and Dra

O-Two Medical Technologies, Inc., Mississauga, CA / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K051889 is the FDA 510(k) clearance record for CAREVENT CA AND DRA, a class II device, cleared for O-Two Medical Technologies, Inc. on under FDA product code BTL (Ventilator, Emergency, Powered (Resuscitator)). FDA records list 8 510(k) clearances for O-Two Medical Technologies, Inc., from to . As of , FDA records show no recalls naming K051889.

Clearance record

Decision date
Received
(49 days to decision)
Product code
BTL Ventilator, Emergency, Powered (Resuscitator)
Regulation
21 CFR 868.5925
Device class
Class II
Review panel
Anesthesiology
Applicant
O-Two Medical Technologies, Inc. 7575 Kimbel St., Mississauga, CA
510(k) summary
Statement
Third party review
No

Clearances, product code BTL

Trailing 12 months

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

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