510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K781271Substantially Equivalent

Monitor, Po2, Intravascular

Roche Medical Electronics, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K781271 is the FDA 510(k) clearance record for MONITOR, PO2, INTRAVASCULAR, a class II device, cleared for Roche Medical Electronics, Inc. on under FDA product code CCE (Analyzer, Gas, Oxygen, Partial Pressure, Blood-Phase, Indwelling). FDA records list 16 510(k) clearances for Roche Medical Electronics, Inc., from to . As of , FDA records show no recalls naming K781271.

Clearance record

Decision date
Received
(80 days to decision)
Product code
CCE Analyzer, Gas, Oxygen, Partial Pressure, Blood-Phase, Indwelling
Regulation
21 CFR 868.1200
Device class
Class II
Review panel
Anesthesiology
Applicant
Roche Medical Electronics, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code CCE

Trailing 12 months

FDA records hold no clearances under product code CCE in the trailing twelve months.

FDA records show no clearances under product code CCE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code CCE, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260