510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K780571Substantially Equivalent

Blood Pressure Module

C-V Monitors Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K780571 is the FDA 510(k) clearance record for BLOOD PRESSURE MODULE, a class II device, cleared for C-V Monitors Corp. on under FDA product code DRQ (Amplifier And Signal Conditioner, Transducer Signal). FDA records list 5 510(k) clearances for C-V Monitors Corp., from to . As of , FDA records show no recalls naming K780571.

Clearance record

Decision date
Received
(29 days to decision)
Product code
DRQ Amplifier And Signal Conditioner, Transducer Signal
Regulation
21 CFR 870.2060
Device class
Class II
Review panel
Cardiovascular
Applicant
C-V Monitors Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DRQ

Trailing 12 months

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

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