510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K901785Substantially Equivalent

Newport Wave Ventilator Model E200

Newport Medical Instruments, Inc., Newport Beach CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K901785 is the FDA 510(k) clearance record for NEWPORT WAVE VENTILATOR MODEL E200, 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 no recalls naming K901785.

Clearance record

Decision date
Received
(114 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. P.O. Box 2600, Newport Beach 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