510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K071195Substantially Equivalent

Khbs (Krishnamurthy Hepato-Biliary Software), Model Version 1.5

Ani-Kal Ii, LLC, Portland OR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K071195 is the FDA 510(k) clearance record for KHBS (KRISHNAMURTHY HEPATO-BILIARY SOFTWARE), MODEL VERSION 1.5, a class I device, cleared for Ani-Kal Ii, LLC on under FDA product code IYX (Camera, Scintillation (Gamma)). FDA records list one 510(k) clearance for Ani-Kal Ii, LLC. As of , FDA records show no recalls naming K071195.

Clearance record

Decision date
Received
(51 days to decision)
Product code
IYX Camera, Scintillation (Gamma)
Regulation
21 CFR 892.1100
Device class
Class I
Review panel
Radiology
Applicant
Ani-Kal Ii, LLC 7570 SW W. Gate Way, Portland OR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code IYX

Trailing 12 months

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

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