510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K940739Substantially Equivalent

Newport Communicat Protocol Interface Adaptor

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

K940739 is the FDA 510(k) clearance record for NEWPORT COMMUNICAT PROTOCOL INTERFACE ADAPTOR, a class II device, cleared for Newport Medical Instruments, Inc. on under FDA product code MOD (Accessory To Continuous Ventilator (Respirator)). FDA records list 23 510(k) clearances for Newport Medical Instruments, Inc., from to . As of , FDA records show no recalls naming K940739.

Clearance record

Decision date
Received
(383 days to decision)
Product code
MOD Accessory To Continuous Ventilator (Respirator)
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
510(k) summary
Statement
Third party review
No

Clearances, product code MOD

Trailing 12 months
3 clearances under product code MOD in the twelve months to October 2026, August 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code MOD, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20262
September 20260
October 20260