Cat-600 Penile Plethysmograph

No FDA recalls found in the data synced 9 Oct 2026.

510(k) Number

K936115 ↗

FDA Product Code

LIL

Device Class

U

Advisory Committee

Unknown

FDA Decision

SESE Substantially Equivalent

• Bi-4520 Dual Impedometer

  Not classified

  FDA 510(k) K821723 Active Cleared 15 Sep 1982

• Pp-100, Personal Perineometer

  Class II

  FDA 510(k) K821664 Active Cleared 13 Jul 1982

• Stimulator, Sonic Control (As-1)

  Class II

  FDA 510(k) K760166 Active Cleared 20 Jul 1976

• Cat-400ul Penile Plethysmograph

  Unclassified

  FDA 510(k) K940128 Active Cleared 10 Jan 1995

• Visualax

  Class II

  FDA 510(k) K781634 Active Cleared 3 Oct 1978

• A Sleep Assessment Device

  Class II

  FDA 510(k) K792305 Active Cleared 20 Dec 1979