DISPOSABLE HOLDER FOR HANCOCK MITRAL— 510(k) K811235

Name: FDA 510(k) clearance K811235
Creator: U.S. Food and Drug Administration
Published: 1981-05-13

Substantially Equivalent

Vascor, Inc.

FDA 510(k) clearance K811235 for DISPOSABLE HOLDER FOR HANCOCK MITRAL, Substantially Equivalent on 1981-05-13. Applicant: Vascor, Inc.. Device class: 1.

Clearance details

Applicant: Vascor, Inc.
Product code: Code DTJ
Device class: Class 1
Regulation: 21 CFR 870.3935
Advisory panel: Cardiovascular
Date received: 1981-05-04
Decision date: 1981-05-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DTJ

view all

K962154 — CARBOMEDICS HANDLE1996-08-27
K960169 — CARBOMEDICS VALVE TESTER1996-04-15
K944214 — BAXTER HANDLE MODEL 11501995-02-10
K942736 — CARBOMEDICS(R) PROSTHETIC HEART VALVE HOLDER HANDLE1994-07-06
K880052 — EDWARDS-DUROMEDICS MITRAL VALVE ROTATOR1988-04-01

More clearances from Vascor, Inc.

view all

K811236 — DISPOSABLE HOLDER FOR HANCOCK AORTIC1981-05-13

Data sourced from openFDA. This site is unofficial and independent of the FDA.