510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K893232Substantially Equivalent

Model V420 Direct Pressure Monitor & 427 Waveform

Camino Laboratories, Inc., San Diego CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K893232 is the FDA 510(k) clearance record for MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORM, a class II device, cleared for Camino Laboratories, Inc. on under FDA product code DSK (Computer, Blood-Pressure). FDA records list 18 510(k) clearances for Camino Laboratories, Inc., from to . As of , FDA records show no recalls naming K893232.

Clearance record

Decision date
Received
(77 days to decision)
Product code
DSK Computer, Blood-Pressure
Regulation
21 CFR 870.1110
Device class
Class II
Review panel
Cardiovascular
Applicant
Camino Laboratories, Inc. 5955 Pacific Center Blvd., San Diego CA
Third party review
No

Clearances, product code DSK

Trailing 12 months

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

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