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510(k) K890047

VASCUCARE PERCUTANEOUS ANGIOSCOPY DELIVERY SYSTEM by Vascucare, Inc. — Product Code LYK

K890047 is an FDA 510(k) premarket notification submitted by Vascucare, Inc. for the device "VASCUCARE PERCUTANEOUS ANGIOSCOPY DELIVERY SYSTEM". The FDA issued a decision of Substantially Equivalent on June 20, 1989. The device falls under product code LYK (Angioscope), a Class II device regulated under 21 CFR 876.1500. Vascucare, Inc. has at least 2 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 20, 1989
Date Received
January 5, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Angioscope
Device Class
Class II
Regulation Number
876.1500
Review Panel
CV
Submission Type

Other clearances by Vascucare, Inc.

  • K883158 — RESPIRATORY AIRWAY TUBE MONITOR (RATM) (March 6, 1989)
  • K881780 — VASCUCARE ANGIOPUMP (September 28, 1988)

Other clearances for product code LYK

  • K253842 — Vena MicroAngioscope™ System (January 28, 2026)
  • K251767 — Vena MicroAngioscope™ System (October 1, 2025)
  • K062340 — CARDIOOPTICS AUGMENTATIVE CARDIAC OPTICAL IMAGING SYSTEM (November 30, 2006)
  • K050808 — CORONARY SINUS ACCESS KIT, MODEL KCS8F-01 (July 28, 2005)
  • K011793 — KSEA FIBERSCOPE (April 17, 2002)
  • K012724 — SMITH & NEPHEW VASCULAR VIDEOENDOSCOPE SYSTEM, MODEL 7209273 (November 8, 2001)
  • K001408 — KSEA VASCULAR FIBERSCOPES (October 30, 2000)
  • K964061 — GORE ANGIOSCOPIC VALVVLOTOME KIT (TBD) (February 20, 1997)
  • K952638 — 4.5F IMAGECATH CORONARY ANGIOSCOPE, MODEL COV45 [SUBSEQUENTLY REFERRED TO AS THE (July 28, 1995)
  • K951721 — APPLIED MEDICAL 1.5MM REUSABLE ANGIOSCOPE (July 11, 1995)

FDA data resources