510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K032831Substantially Equivalent

Pro 2 Monitor, Pro 2 Sensor, Pro2 Holder, Pro2 Neonate Holder, Models, Pro- 200, Ans-200, Ahl-200, Nhl-200

ConMed Corporation, Utica NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K032831 is the FDA 510(k) clearance record for PRO 2 MONITOR, PRO 2 SENSOR, PRO2 HOLDER, PRO2 NEONATE HOLDER, MODELS, PRO- 200, ANS-200, AHL-200, NHL-200, a class II device, cleared for Conmed Corporation on under FDA product code DQA (Oximeter). FDA records list 84 510(k) clearances for Conmed Corporation, from to . As of , FDA records show no recalls naming K032831.

Clearance record

Decision date
Received
(355 days to decision)
Product code
DQA Oximeter
Regulation
21 CFR 870.2700
Device class
Class II
Review panel
Cardiovascular
Applicant
Conmed Corporation 525 French Rd., Utica NY
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DQA

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