510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K874615Substantially Equivalent

Laser Cannister Filter

Medical Marketing, Inc., Fischer TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K874615 is the FDA 510(k) clearance record for LASER CANNISTER FILTER, a class II device, cleared for Medical Marketing, Inc. on under FDA product code HHR (Laser, Surgical, Gynecologic). FDA records list 4 510(k) clearances for Medical Marketing, Inc. As of , FDA records show no recalls naming K874615.

Clearance record

Decision date
Received
(227 days to decision)
Product code
HHR Laser, Surgical, Gynecologic
Regulation
21 CFR 884.4550
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Medical Marketing, Inc. P.O. Box 222, Fischer TX
Third party review
No

Clearances, product code HHR

Trailing 12 months

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

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