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510(k) K890515

PERIPHERAL ATHERECTOMY SYSTEM by Intensive Technology, Inc. — Product Code DWX

K890515 is an FDA 510(k) premarket notification submitted by Intensive Technology, Inc. for the device "PERIPHERAL ATHERECTOMY SYSTEM". The FDA issued a decision of Substantially Equivalent on May 23, 1989. The device falls under product code DWX (Stripper, Artery, Intraluminal), a Class II device regulated under 21 CFR 870.4875. Intensive Technology, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 23, 1989
Date Received
February 1, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stripper, Artery, Intraluminal
Device Class
Class II
Regulation Number
870.4875
Review Panel
CV
Submission Type

Other clearances by Intensive Technology, Inc.

  • K922970 — INTRA-OPERATIVE TEC ATHERECTOMY SYSTEM (January 13, 1993)
  • K912664 — TEC ROTATING DUAL HEMOVALVE (August 24, 1992)
  • K911869 — IVT GUIDING CATHETER (October 16, 1991)
  • K903463 — IVT INTRODUCER SHEATH (January 3, 1991)
  • K904003 — HEMOCHRON(R) HEPARIN RESPONSE TEST (November 29, 1990)
  • K901767 — MODIFIED IVT PERIPHERAL ATHERECTOMY (June 28, 1990)
  • K896403 — MODIFIED IVT PERIPHERAL ATHERECTOMY SYSTEM (March 6, 1990)
  • K895903 — IVT 0.014 GUIDE WIRE (January 4, 1990)
  • K892209 — APTT BY HEMOCHRON(R) (June 22, 1989)
  • K882804 — 0.014 PERIPHERAL GUIDE WIRE (October 28, 1988)

Other clearances for product code DWX

  • K121415 — MOLLRING MULTITASC (September 5, 2012)
  • K032105 — ENDOHELIX ENDARTERECTOMY DEVICE (October 30, 2003)
  • K020925 — CARBODISSECTING ENDOSCOPE (April 29, 2003)
  • K003719 — VASCULAR ARCHITECTS PERISCOPE DEVICE (February 28, 2001)
  • K950813 — MOLLRING CUTTER (July 25, 1995)
  • K933498 — EXTERNAL VEIN STRIPPER (March 23, 1994)
  • K913803 — INTRALUMINAL ARTERY STRIPPER (April 24, 1992)
  • K911099 — MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE (June 25, 1991)
  • K904944 — TRANSLUMINAL ENDARTERECTOMY DEVICE (December 17, 1990)
  • K895878 — OLYMPUS VALVULOTOME W/DETACHABLE TIP (January 2, 1990)

FDA data resources