Applicator, Angiography (7310MOBIN-Uddin)

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

510(k) Number

K760151 ↗

FDA Product Code

DTK

Device Class

Class II

Regulation

21 CFR Part 870.3375

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Filter (7220&7221 Mobin-Uddin Vena Cava)

  Class II

  FDA 510(k) K760152 Active Cleared 19 Jul 1976

• Model 100 Spectraview

  Class I

  FDA 510(k) K800655 Active Cleared 16 Apr 1980

• Ac Adapter:models 9525, 9526, 9527

  Class II

  FDA 510(k) K781535 Active Cleared 15 Sep 1978

• Carpentier-Edwards Flex. Annuloplasty

  Class II

  FDA 510(k) K792441 Active Cleared 17 Mar 1980

• Probe & Catheter

  Class II

  FDA 510(k) K771663 Active Cleared 20 Sep 1977

• Disposable Holder for Bioprosthesis

  Class I

  FDA 510(k) K790022 Active Cleared 15 Jan 1979

See all devices from Edwards Laboratories →