510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K820720Substantially Equivalent

Respirator Monitor

Rv Systems, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K820720 is the FDA 510(k) clearance record for RESPIRATOR MONITOR, a class II device, cleared for Rv Systems on under FDA product code CAP (Monitor, Airway Pressure (Includes Gauge And/Or Alarm)). FDA records list one 510(k) clearance for Rv Systems. As of , FDA records show no recalls naming K820720.

Clearance record

Decision date
Received
(41 days to decision)
Product code
CAP Monitor, Airway Pressure (Includes Gauge And/Or Alarm)
Regulation
21 CFR 868.2600
Device class
Class II
Review panel
Anesthesiology
Applicant
Rv Systems 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code CAP

Trailing 12 months

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

FDA records show no clearances under product code CAP in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code CAP, 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