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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K992133Substantially Equivalent - Subject to Tracking Reg.

Newport Ht50 Ventilator with Humidifier Ht50-H, Newport Ht50 Ventilator without Humidifier, Ht50-H1, Newport Ht50 Ventil

Newport Medical Instruments, Inc., Costa Mesa CA / Traditional, Substantially Equivalent - Subject to Tracking Reg.
FDA source (opens on fda.gov)

K992133 is the FDA 510(k) clearance record for NEWPORT HT50 VENTILATOR WITH HUMIDIFIER HT50-H, NEWPORT HT50 VENTILATOR WITHOUT HUMIDIFIER, HT50-H1, NEWPORT HT50 VENTIL, a class II device, cleared for Newport Medical Instruments, Inc. on under FDA product code CBK (Ventilator, Continuous, Facility Use). FDA records list 23 510(k) clearances for Newport Medical Instruments, Inc., from to . As of , FDA records show 5 recalls naming K992133.

Clearance record

Decision date
Received
(408 days to decision)
Product code
CBK Ventilator, Continuous, Facility Use
Regulation
21 CFR 868.5895
Device class
Class II
Review panel
Anesthesiology
Applicant
Newport Medical Instruments, Inc. 760 W 16th St., Bldg. N, Costa Mesa CA
Third party review
No

Clearances, product code CBK

Trailing 12 months
4 clearances under product code CBK in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code CBK, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20261
April 20261
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260