Vagi-Press #401

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K790851 ↗

FDA Product Code

KOH

Device Class

Class I

Regulation

21 CFR Part 884.4520

Advisory Committee

Obstetrics/Gynecology

FDA Decision

SESE Substantially Equivalent

• Forceps #101 and #102

  Class I

  FDA 510(k) K790854 Active Cleared 5 Jun 1979

• Proctoscope #501

  Class II

  FDA 510(k) K790856 Active Cleared 29 May 1979

• Easy-Spec

  Class II

  FDA 510(k) K790853 Active Cleared 30 Jul 1979

• Vagi-Spec

  Class II

  FDA 510(k) K790852 Active Cleared 30 Jul 1979

• Catheterization Forcep

  Class I

  FDA 510(k) K792494 Active Cleared 20 Dec 1979

• Surgical Drape Clip #201

  Class I

  FDA 510(k) K790855 Active Cleared 3 Aug 1979