510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K960426Substantially Equivalent

Medicomp Flexi-Smooth Wound Drainage Catheter

Medical Components, Inc., Harleysville PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K960426 is the FDA 510(k) clearance record for MEDICOMP FLEXI-SMOOTH WOUND DRAINAGE CATHETER, a class I device, cleared for Medical Components, Inc. on under FDA product code GBW (Catheter, Peritoneal). FDA records list 72 510(k) clearances for Medical Components, Inc., from to . As of , FDA records show no recalls naming K960426.

Clearance record

Decision date
Received
(52 days to decision)
Product code
GBW Catheter, Peritoneal
Regulation
21 CFR 878.4200
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Medical Components, Inc. 1499 Delp Dr., Harleysville PA
510(k) summary
Statement
Third party review
No

Clearances, product code GBW

Trailing 12 months

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

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