Model 1000 Apc-Angioplasty Pressure

FDA 510(k) K841493 · E.A. Fischione Instrument Mfg.

Substantially Equivalent

510(k) numberK841493

Submission

Device name
Model 1000 Apc-Angioplasty Pressure
Applicant
E.A. Fischione Instrument Mfg.
Mchenry, IL, US
Received
April 10, 1984
Decision date
June 11, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DXT – Injector And Syringe, Angiographic
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1650
Specialty
Cardiovascular

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K252652Disposable Syringes with Accessories for Power Injectors (900103T); Disposable Syringes…DXT · Traditional Fortis Biosolutions Company Limited05/14/2026SE
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K252638VeraPro S100 Multi-Use Syringe (018808); VeraPro S100 LV1 Low Viscosity Single-Use…DXT · Traditional Acist Medical Systems, Inc.05/13/2026SE
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K251788Extension tubeDXT · Traditional Zhuhai DR Medical Instruments Co., Ltd.03/05/2026SE
K252891MEDRAD MRXperion MR Injection System and MR Injection System Syringe Kit; MEDRAD ISI2…DXT · Traditional Bayer Medical Care, Inc.02/13/2026SE
K244038High Pressure TubingDXT · Traditional Shandong Int Medical Instruments Co., Ltd.09/05/2025SE
K242143Angiography InjectorDXT · Traditional Shandong Int Medical Instruments Co., Ltd.12/23/2024SE
K242212Disposable Syringe (Kit); Nemoto Disposable Syringe (Kit)DXT · Traditional Nemoto Kyorindo Co., Ltd.08/27/2024SE
K241109Single-use Sterile High-pressure Angiographic Syringes and AccessoriesDXT · Traditional Shenzhen Boon Medical Supply Co., Ltd.08/22/2024SE

More from Shenzhen Boon Medical Supply Co., Ltd.

510(k)DeviceDecision
K853136Model 1100 Apc(Angioplasty Pressure Controller)MAV · Traditional 12/03/1985SE

Questions and answers

When was Model 1000 Apc-Angioplasty Pressure cleared by the FDA?

Model 1000 Apc-Angioplasty Pressure (K841493) received a 510(k) decision of Substantially Equivalent on June 11, 1984, 62 days after the submission was received.

What is the product code of K841493?

The FDA product code is DXT – Injector And Syringe, Angiographic, a Class II (moderate risk) device regulated under 21 CFR 870.1650.