510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K902555Substantially Equivalent

Amcath Coagulation Probe

Intl. Medical, Inc., Danielson CT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K902555 is the FDA 510(k) clearance record for AMCATH COAGULATION PROBE, a class II device, cleared for Intl. Medical, Inc. on under FDA product code HFG (Coagulator, Laparoscopic, Unipolar (And Accessories)). FDA records list 17 510(k) clearances for Intl. Medical, Inc., from to . As of , FDA records show no recalls naming K902555.

Clearance record

Decision date
Received
(12 days to decision)
Product code
HFG Coagulator, Laparoscopic, Unipolar (And Accessories)
Regulation
21 CFR 884.4160
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Intl. Medical, Inc. 175 Connecticut Mills Ave., Danielson CT
Third party review
No

Clearances, product code HFG

Trailing 12 months

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

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