510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K071642Substantially Equivalent

Mediaid M960 Series, Vital Signs Monitor and Mediaid M900 Series, Pulse Oximeter

Mediaid, Inc., Cerritos CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K071642 is the FDA 510(k) clearance record for MEDIAID M960 SERIES, VITAL SIGNS MONITOR AND MEDIAID M900 SERIES, PULSE OXIMETER, a class II device, cleared for Mediaid, Inc. on under FDA product code DQA (Oximeter). FDA records list 4 510(k) clearances for Mediaid, Inc., from to . As of , FDA records show no recalls naming K071642.

Clearance record

Decision date
Received
(319 days to decision)
Product code
DQA Oximeter
Regulation
21 CFR 870.2700
Device class
Class II
Review panel
Cardiovascular
Applicant
Mediaid, Inc. 17517 Fabrica Way, Suite H, Cerritos CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DQA

Trailing 12 months
12 clearances under product code DQA in the twelve months to October 2026, December 2025 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code DQA, trailing twelve months
MonthClearances
November 20252
December 20253
January 20261
February 20262
March 20260
April 20261
May 20263
June 20260
July 20260
August 20260
September 20260
October 20260