Silastic Brand Percutaneous Skin Expande

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K801042 ↗

FDA Product Code

LCJ

Device Class

U

Advisory Committee

Unknown

FDA Decision

SESE Substantially Equivalent

• Silastic Scleral Sponge II W/Circling Bd

  Class II

  FDA 510(k) K800140 Active Cleared 3 Mar 1980

• Silastic U-Tube Kit

  Class I

  FDA 510(k) K781526 Active Cleared 20 Sep 1978

• Silastic Brand Q7-2091 Gastric Sump Tube

  Class II

  FDA 510(k) K760708 Active Cleared 23 Nov 1976

• Silastic Percutaneous Gastrointest. Tube

  Class II

  FDA 510(k) K760945 Active Cleared 23 Nov 1976

• Silastic Bone Plug H.P.(Cement Restrict)

  Class II

  FDA 510(k) K800898 Active Cleared 2 May 1980

• Implant, H.P. Condylar

  Class II

  FDA 510(k) K781870 Active Cleared 9 Feb 1979

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