510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K895084Substantially Equivalent

Aperture

Custom Medical Products, Ltd., Deer Park NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K895084 is the FDA 510(k) clearance record for APERTURE, a class II device, cleared for Custom Medical Products, Ltd. on under FDA product code IZS (Aperture, Radiographic). FDA records list 14 510(k) clearances for Custom Medical Products, Ltd., from to . As of , FDA records show no recalls naming K895084.

Clearance record

Decision date
Received
(74 days to decision)
Product code
IZS Aperture, Radiographic
Regulation
21 CFR 892.1610
Device class
Class II
Review panel
Radiology
Applicant
Custom Medical Products, Ltd. 19a W. Industry Ct., Deer Park NY
Third party review
No

Clearances, product code IZS

Trailing 12 months

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

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