Angioscope
FDA 510(k) K894459 · Intramed Laboratories, Inc.
510(k) numberK894459
Submission
- Device name
- Angioscope
- Applicant
- Intramed Laboratories, Inc.
San Diego, CA, US - Received
- July 18, 1989
- Decision date
- March 7, 1990
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- LYK – Angioscope
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.1500
- Specialty
- Gastroenterology, Urology
Other 510(k)s with product code LYK
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|---|---|---|---|
| K253842 | Vena MicroAngioscope SystemLYK · Traditional | Vena Medical Holdings Corp | 01/28/2026SE |
| K251767 | Vena MicroAngioscope SystemLYK · Traditional | Vena Medical Holdings Corp | 10/01/2025SE |
| K062340 | Cardiooptics Augmentative Cardiac Optical Imaging SystemLYK · Traditional | Cardio-Optics, Inc. | 11/30/2006SE |
| K050808 | Coronary Sinus Access Kit, Model KCS8F-01LYK · Traditional | Cardio-Optics, Inc. | 07/28/2005SE |
| K011793 | Ksea FiberscopeLYK · Traditional | KARL STORZ Endoscopy-America, Inc. | 04/17/2002SE |
| K012724 | Smith & Nephew Vascular Videoendoscope System, Model 7209273LYK · Traditional | Smith & Nephew, Inc. | 11/08/2001SE |
| K001408 | Ksea Vascular FiberscopesLYK · Traditional | KARL STORZ Endoscopy-America, Inc. | 10/30/2000SE |
| K964061 | Gore Angioscopic Valvvlotome Kit (TBD)LYK · Traditional | W. L. Gore & Associates, Inc. | 02/20/1997SE |
| K952638 | 4.5F Imagecath Coronary Angioscope, Model COV45 [Subsequently Referred to AS the…LYK · Traditional | Baxter Edwards | 07/28/1995SE |
| K951721 | Applied Medical 1.5MM Reusable AngioscopeLYK · Traditional | Applied Medical Resources | 07/11/1995SE |
More from Applied Medical Resources
| 510(k) | Device | Decision |
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| K953258 | Titanium Hemostatic ClipFZP · Traditional | 01/05/1996SE |
| K942457 | Graft Thrombectomy InstrumentsMCW · Traditional | 02/07/1995SE |
| K931792 | ArthroscopeHRH · Traditional | 06/13/1994SE |
| K925283 | ValvulotomeMGZ · Traditional | 02/10/1994SE |
| K934696 | AngioscopeLYK · Traditional | 01/18/1994SE |
| K922114 | Endoscopic Retrieval BasketFFL · Traditional | 08/03/1992SE |
| K914385 | Optical ValvulotomeMGZ · Traditional | 03/02/1992SE |
| K904465 | Flexible ArthroscopeHRX · Traditional | 12/20/1990SE |
| K903528 | LaparoscopeHET · Traditional | 09/04/1990SE |
| K902444 | Clearview(Tm) Angioscopic Irrigation PumpDQI · Traditional | 08/30/1990SE |
Questions and answers
When was Angioscope cleared by the FDA?
Angioscope (K894459) received a 510(k) decision of Substantially Equivalent on March 7, 1990, 232 days after the submission was received.
What is the product code of K894459?
The FDA product code is LYK – Angioscope, a Class II (moderate risk) device regulated under 21 CFR 876.1500.