510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K983250Substantially Equivalent

Invasive Blood Pressure (Ibp) Function, Model 9500 Multigas Monitor

Magnetic Resonance Equipment Corp., Bay Shore NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K983250 is the FDA 510(k) clearance record for INVASIVE BLOOD PRESSURE (IBP) FUNCTION, MODEL 9500 MULTIGAS MONITOR, a class II device, cleared for Magnetic Resonance Equipment Corp. on under FDA product code DSK (Computer, Blood-Pressure). FDA records list 5 510(k) clearances for Magnetic Resonance Equipment Corp., from to . As of , FDA records show one recall naming K983250.

Clearance record

Decision date
Received
(452 days to decision)
Product code
DSK Computer, Blood-Pressure
Regulation
21 CFR 870.1110
Device class
Class II
Review panel
Cardiovascular
Applicant
Magnetic Resonance Equipment Corp. 6 Washington Ave., Bay Shore NY
510(k) summary
Summary
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