Solcovac Wound Drainage System

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K915867 ↗

FDA Product Code

GCY

Device Class

Class I

Regulation

21 CFR Part 878.4680

Advisory Committee

General, Plastic Surgery

FDA Decision

SESK Substantially Equivalent — Kit

• Solcotrans Orthopaedic Drainage/Reinfusion System

  Class II

  FDA 510(k) K913177 Active Cleared 25 Feb 1993

• Solcotrans Chest Drainage Autotransfusion System

  Class II

  FDA 510(k) K872590 Active Cleared 4 Sep 1987

• Hall Vein Stripper

  Class II

  FDA 510(k) K872157 Active Cleared 7 Jul 1987

• Solco Basle Intraoperative Autottrnsfus

  Class II

  FDA 510(k) K843821 Active Cleared 1 Oct 1985

• Solcotrans Intraoperative Autotransfusion System

  Class II

  FDA 510(k) K896858 Active Cleared 5 Apr 1990

• Solcotrans Ortho. Drainage/Reinfusion System

  Class II

  FDA 510(k) K883058 Active Cleared 28 Oct 1988

See all devices from Solco Basle, Inc. →