510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K831750Substantially Equivalent

Pm-3

Delta Medical Industries, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K831750 is the FDA 510(k) clearance record for PM-3, a class II device, cleared for Delta Medical Industries on under FDA product code DXS (Gauge, Pressure, Coronary, Cardiopulmonary Bypass). FDA records list 27 510(k) clearances for Delta Medical Industries, from to . As of , FDA records show no recalls naming K831750.

Clearance record

Decision date
Received
(55 days to decision)
Product code
DXS Gauge, Pressure, Coronary, Cardiopulmonary Bypass
Regulation
21 CFR 870.4310
Device class
Class II
Review panel
Cardiovascular
Applicant
Delta Medical Industries 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DXS

Trailing 12 months

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

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