Carbomedics(R) Prosthetic Heart Valve Holder Handle

FDA 510(k) K942736 · Carbomedics, Inc.

Substantially Equivalent

510(k) numberK942736

Submission

Device name
Carbomedics(R) Prosthetic Heart Valve Holder Handle
Applicant
Carbomedics, Inc.
Austin, TX, US
Received
June 10, 1994
Decision date
July 6, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DTJ – Holder, Heart-Valve, Prosthesis
Device class
Class I (low risk)
Regulation
21 CFR 870.3935
Specialty
Cardiovascular

Other 510(k)s with product code DTJ

510(k)DeviceApplicantDecision
K962154Carbomedics HandleDTJ · Traditional Carbomedics, Inc.08/27/1996SE
K960169Carbomedics Valve TesterDTJ · Traditional Carbomedics, Inc.04/15/1996SE
K944214Baxter Handle Model 1150DTJ · Traditional Baxter Edwards02/10/1995SE
K880052Edwards-Duromedics Mitral Valve RotatorDTJ · Traditional Baxter Healthcare Corp04/01/1988SE
K871596Ionescu-Shiley Pericardial Xenograft (Isu)DTJ · Traditional Shiley, Inc.06/15/1987SE
K864155Modification of Carpentier-Edwards BioprosthesisDTJ · Traditional American Edwards Laboratories11/20/1986SE
K813276Ionescu-Shiley Valve Holder & HandleDTJ · Traditional Shiley, Inc.12/10/1981SE
K811236Disposable Holder for Hancock AorticDTJ · Traditional Vascor, Inc.05/13/1981SE
K811235Disposable Holder for Hancock MitralDTJ · Traditional Vascor, Inc.05/13/1981SE
K792034Integral Disposable Holder CarpentierDTJ · Traditional Edwards Laboratories12/07/1979SE

More from Edwards Laboratories

510(k)DeviceDecision
K970375Annuloflo SystemKRH · Traditional 07/25/1997ST
K964665Vascutek Gelweave Vascular Graft (Bifurcated Configuration)DSY · Traditional 02/19/1997ST
K962154Carbomedics HandleDTJ · Traditional 08/27/1996SE
K960923Carbomedics Mitral RotatorMOP · Traditional 04/29/1996SE
K960706Vascutek Vascusoft Plus Vascular GraftDSY · Traditional 04/25/1996SESP
K960169Carbomedics Valve TesterDTJ · Traditional 04/15/1996SE
K955588Vascutek Graft Sizer SetDSY · Traditional 03/07/1996ST
K952184Carbomedics Supra-Annular Valve SizerDTI · Traditional 11/29/1995SE
K951368Carbomedics Exended Mitral RotatorMOP · Traditional 06/20/1995SE
K934951Valve SizerDTI · Traditional 12/10/1993SE

Questions and answers

When was Carbomedics(R) Prosthetic Heart Valve Holder Handle cleared by the FDA?

Carbomedics(R) Prosthetic Heart Valve Holder Handle (K942736) received a 510(k) decision of Substantially Equivalent on July 6, 1994, 26 days after the submission was received.

What is the product code of K942736?

The FDA product code is DTJ – Holder, Heart-Valve, Prosthesis, a Class I (low risk) device regulated under 21 CFR 870.3935.