510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K902628Substantially Equivalent

Interflo Medical Model Interflo/1 Cardiac Output

Biometric Research Institute, Inc., Arlington VA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K902628 is the FDA 510(k) clearance record for INTERFLO MEDICAL MODEL INTERFLO/1 CARDIAC OUTPUT, a class II device, cleared for Biometric Research Institute, Inc. on under FDA product code DXG (Computer, Diagnostic, Pre-Programmed, Single-Function). FDA records list 2 510(k) clearances for Biometric Research Institute, Inc. As of , FDA records show one recall naming K902628.

Clearance record

Decision date
Received
(257 days to decision)
Product code
DXG Computer, Diagnostic, Pre-Programmed, Single-Function
Regulation
21 CFR 870.1435
Device class
Class II
Review panel
Cardiovascular
Applicant
Biometric Research Institute, Inc. 1401 Wilson Blvd., Arlington VA
Third party review
No

Clearances, product code DXG

Trailing 12 months
1 clearance under product code DXG in the twelve months to October 2026, February 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DXG, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260