Interpro Int'l, Inc. Isolation Gown

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K874766 ↗

FDA Product Code

FYC

Device Class

Class II

Regulation

21 CFR Part 878.4040

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Patient Examination Gloves (Latex)

  Class I

  FDA 510(k) K891438 Active Cleared 31 May 1989

• Vinyl Examination Gloves (Mfg. Salzgitter Morex)

  Class I

  FDA 510(k) K890968 Active Cleared 31 Jul 1989

• Latex Examination Gloves (Mfg. Ningbo Medical)

  Class I

  FDA 510(k) K890891 Active Cleared 14 Jul 1989

• Laparotomy Sponges

  Unclassified

  FDA 510(k) K874065 Active Cleared 4 Nov 1987

• Surgical Caps

  Class I

  FDA 510(k) K874066 Active Cleared 4 Nov 1987

• Guaze Sponges

  Unclassified

  FDA 510(k) K874067 Active Cleared 14 Dec 1987

See all devices from Interpro Intl., Inc. →