510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K923813Substantially Equivalent

Philips Integris V3000 Rotational Angio Function

Philips North America LLC, 5680 Da Best, NL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K923813 is the FDA 510(k) clearance record for PHILIPS INTEGRIS V3000 ROTATIONAL ANGIO FUNCTION, a class II device, cleared for Philips Medical Systems, Inc. on under FDA product code IZI (System, X-Ray, Angiographic). FDA records list 680 510(k) clearances for Philips North America LLC, from to . As of , FDA records show one recall naming K923813.

Clearance record

Decision date
Received
(79 days to decision)
Product code
IZI System, X-Ray, Angiographic
Regulation
21 CFR 892.1600
Device class
Class II
Review panel
Radiology
Applicant
Philips Medical Systems, Inc. Veenpluis 4-6, 5680 Da Best, NL
510(k) summary
Summary
Third party review
No

Clearances, product code IZI

Trailing 12 months
2 clearances under product code IZI in the twelve months to October 2026, May 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code IZI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20262
June 20260
July 20260
August 20260
September 20260
October 20260