Angiomedics Cath Sheath Introduc W/Hemostasis Valv

FDA 510(k) K861238 · Angiomedics, Inc.

Substantially Equivalent

510(k) numberK861238

Submission

Device name
Angiomedics Cath Sheath Introduc W/Hemostasis Valv
Applicant
Angiomedics, Inc.
Minneapolis, MN, US
Received
April 2, 1986
Decision date
July 16, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DYB – Introducer, Catheter
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1340
Specialty
Cardiovascular

Other 510(k)s with product code DYB

510(k)DeviceApplicantDecision
K253526NAMIC Dilator and SheathDYB · Traditional Medline Industries, LP07/29/2026SE
K261529Micropuncture Kit / Micropuncture Access Kit / Micropuncture Introducer Set/…DYB · Traditional Hartman Medical Group, LLC07/06/2026SE
K261242SimplGuideDYB · Traditional Pendracare06/25/2026SE
K261950Health Line Tearaway IntroducerDYB · Traditional Health Line International Corporation06/22/2026SE
K261492FieldFlex Steerable SheathDYB · Special CenterPoint Systems, LLC06/05/2026SE
K260606Echo Large Bore Introducer SheathDYB · Traditional Echo Medical, LLC04/29/2026SE
K254248Introducer Sheath SetDYB · Traditional Cardiocycle Medical(Suzhou) Co., Ltd.04/23/2026SE
K254279Edwards eSheath+ introducer setDYB · Traditional Edwards Lifesciences04/17/2026SE
K260091Aventus Introducer SheathDYB · Traditional Inquis Medical04/13/2026SE
K260839Protaryx Transseptal Puncture Device (PTX2-001)DYB · Traditional Protaryx Medical, Inc.04/10/2026SE

More from Protaryx Medical, Inc.

510(k)DeviceDecision
K873195Schneider-Shiley Angioport(Tm) Ptca Intro W/HemoDYB · Traditional 12/15/1987SE
K872542Schneider-Shiley Softrac-Pta(Tm) Angio. CatheterLIT · Traditional 09/14/1987SE
K872472Schneider-Shiley Biflator Balloon Inflation DeviceDXT · Traditional 09/14/1987SE
K863342Softip Coronary Sinus Cardioplegia CatheterDWF · Traditional 03/03/1987SE
K852872Angiomedics Softip CatheterDQO · Traditional 10/11/1985SE
K850271Angiomedic's Catheter-Diagnostic IntravascularDQO · Traditional 04/03/1985SE
K834275Softip CatheterDQO · Traditional 02/04/1984SE

Questions and answers

When was Angiomedics Cath Sheath Introduc W/Hemostasis Valv cleared by the FDA?

Angiomedics Cath Sheath Introduc W/Hemostasis Valv (K861238) received a 510(k) decision of Substantially Equivalent on July 16, 1986, 105 days after the submission was received.

What is the product code of K861238?

The FDA product code is DYB – Introducer, Catheter, a Class II (moderate risk) device regulated under 21 CFR 870.1340.