510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K973115Substantially Equivalent

Arripro 35 St/tv

Arnold & Richter Cine Technik, Munich, DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K973115 is the FDA 510(k) clearance record for ARRIPRO 35 ST/TV, a class I device, cleared for Arnold & Richter Cine Technik on under FDA product code IXC (Illuminator, Radiographic-Film). FDA records list 2 510(k) clearances for Arnold & Richter Cine Technik, from to . As of , FDA records show no recalls naming K973115.

Clearance record

Decision date
Received
(13 days to decision)
Product code
IXC Illuminator, Radiographic-Film
Regulation
21 CFR 892.1890
Device class
Class I
Review panel
Radiology
Applicant
Arnold & Richter Cine Technik Turkenstrasse 89, Munich, DE
510(k) summary
Summary
Third party review
Yes

Clearances, product code IXC

Trailing 12 months

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

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