Vascular Biopsy Forceps

FDA 510(k) K910840 · Vascular Products, Inc.

Substantially Equivalent

510(k) numberK910840

Submission

Device name
Vascular Biopsy Forceps
Applicant
Vascular Products, Inc.
Tarpon Springs, FL, US
Received
February 27, 1991
Decision date
July 15, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DWZ – Device, Biopsy, Endomyocardial
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4075
Specialty
Cardiovascular

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K252722Biopsy ForcepsDWZ · Special Fehling Instruments GmbH09/30/2025SE
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K072051Novatome, Model: SU101-50DWZ · Traditional Scholten Surgical Instruments, Inc.10/03/2007SE
K010473Sparrowhawk DisposableDWZ · Traditional Atc Technologies, Inc.06/06/2001SE
K000409Modification to T-Rex Biopsy ForcepsDWZ · Special Boston Scientific Corp02/28/2000SE
K991486Ultra-CbxDWZ · Traditional Medcanica, Inc.11/05/1999SE
K974175Heartport Endoaortic Clamp CatheterDWZ · Traditional Heartport, Inc.12/16/1997SE
K973818T-Rex Biopsy ForcepsDWZ · Traditional Boston Scientific Corp12/16/1997SE
K951447Dynabite Cardiovascular Biopsy ForcepsDWZ · Traditional Portlyn Corp.07/27/1995SE
K933235Cordis Bipal 7 /Biopsy & Bipal Biopsy Forceps, ModifDWZ · Traditional Cordis Corp.01/06/1994SE

More from Cordis Corp.

510(k)DeviceDecision
K913733Sterile Chest TubeGBW · Traditional 10/08/1991SE
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Questions and answers

When was Vascular Biopsy Forceps cleared by the FDA?

Vascular Biopsy Forceps (K910840) received a 510(k) decision of Substantially Equivalent on July 15, 1991, 138 days after the submission was received.

What is the product code of K910840?

The FDA product code is DWZ – Device, Biopsy, Endomyocardial, a Class II (moderate risk) device regulated under 21 CFR 870.4075.