510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K935157Substantially Equivalent

Articulated, Laparoscopic, and Side-Viewing T-Probes

Regulatory Consultants to the Medical Device Indus, Sandy UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K935157 is the FDA 510(k) clearance record for ARTICULATED, LAPAROSCOPIC, AND SIDE-VIEWING T-PROBES, a class II device, cleared for Regulatory Consultants TO the Medical Device Indus on under FDA product code KPX (Changer, Radiographic Film/Cassette). FDA records list one 510(k) clearance for Regulatory Consultants TO the Medical Device Indus. As of , FDA records show no recalls naming K935157.

Clearance record

Decision date
Received
(285 days to decision)
Product code
KPX Changer, Radiographic Film/Cassette
Regulation
21 CFR 892.1860
Device class
Class II
Review panel
Radiology
Applicant
Regulatory Consultants TO the Medical Device Indus 9712 S. Altamont Dr., Sandy UT
510(k) summary
Statement
Third party review
No

Clearances, product code KPX

Trailing 12 months

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

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