510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K873115Substantially Equivalent

Cabot Fiber Laser Probe

Cabot Medical Corp., Langhorne PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K873115 is the FDA 510(k) clearance record for CABOT FIBER LASER PROBE, a class II device, cleared for Cabot Medical Corp. on under FDA product code HET (Laparoscope, Gynecologic (And Accessories)). FDA records list 38 510(k) clearances for Cabot Medical Corp., from to . As of , FDA records show no recalls naming K873115.

Clearance record

Decision date
Received
(171 days to decision)
Product code
HET Laparoscope, Gynecologic (And Accessories)
Regulation
21 CFR 884.1720
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Cabot Medical Corp. 2021 Cabot Blvd. W., Langhorne PA
Third party review
No

Clearances, product code HET

Trailing 12 months

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

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