510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K001388Substantially Equivalent

Data Master Perfusion Monitoring System

Dideco S.p.A., North Attleboro MA / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)

K001388 is the FDA 510(k) clearance record for DATA MASTER PERFUSION MONITORING SYSTEM, a class II device, cleared for Dideco on under FDA product code DRY (Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass). FDA records list 33 510(k) clearances for Dideco, from to . As of , FDA records show no recalls naming K001388.

Clearance record

Decision date
Received
(87 days to decision)
Product code
DRY Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass
Regulation
21 CFR 870.4330
Device class
Class II
Review panel
Cardiovascular
Applicant
Dideco 49 Plain St., North Attleboro MA
510(k) summary
Summary
Third party review
No

Clearances, product code DRY

Trailing 12 months

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

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