510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K930124Substantially Equivalent

Variant of Octostop and Octopaque

Octostop, Inc., Montreal, Qc., CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K930124 is the FDA 510(k) clearance record for VARIANT OF OCTOSTOP AND OCTOPAQUE, a class I device, cleared for Octostop, Inc. on under FDA product code KXH (Cradle, Patient, Radiologic). FDA records list 13 510(k) clearances for Octostop, Inc., from to . As of , FDA records show no recalls naming K930124.

Clearance record

Decision date
Received
(393 days to decision)
Product code
KXH Cradle, Patient, Radiologic
Regulation
21 CFR 892.1830
Device class
Class I
Review panel
Radiology
Applicant
Octostop, Inc. Casier Postal 1476, Montreal, Qc., CA
510(k) summary
Statement
Third party review
No

Clearances, product code KXH

Trailing 12 months

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

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