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510(k) K904909

I/A VITROPHAGE MODEL YPR 2001 by Visioncare Devices, Inc. — Product Code HQE

K904909 is an FDA 510(k) premarket notification submitted by Visioncare Devices, Inc. for the device "I/A VITROPHAGE MODEL YPR 2001". The FDA issued a decision of Substantially Equivalent on January 28, 1991. The device falls under product code HQE (Instrument, Vitreous Aspiration And Cutting, Ac-Powered), a Class II device regulated under 21 CFR 886.4150. Visioncare Devices, Inc. has at least 5 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 28, 1991
Date Received
October 31, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Instrument, Vitreous Aspiration And Cutting, Ac-Powered
Device Class
Class II
Regulation Number
886.4150
Review Panel
OP
Submission Type

Other clearances by Visioncare Devices, Inc.

  • K212763 — UniVit HE, UniVit UHS (August 10, 2022)
  • K120170 — PROCARE PLUS VITRECTOMY SYSTEM (May 30, 2012)
  • K023939 — VELOCITY ADVANTAGE (April 17, 2003)
  • K971064 — BAYERS BIMANUAL I/A HANDPIECES (June 9, 1997)
  • K940746 — VIT CUTTER MODEL 94 (June 6, 1994)

Other clearances for product code HQE

  • K212763 — UniVit HE, UniVit UHS (August 10, 2022)
  • K170183 — Cetus system, Cetus probe (September 27, 2017)
  • K153168 — Bi-Blade Vitrectomy Cutter (April 29, 2016)
  • K141065 — CONSTELLATION VISION SYSTEM (August 22, 2014)
  • K121675 — VERSAVIT (June 21, 2012)
  • K120170 — PROCARE PLUS VITRECTOMY SYSTEM (May 30, 2012)
  • K102222 — ULTIMATE VIT ENHAMCER (UVE) (April 8, 2011)
  • K033390 — COLIBRI DISPOSABLE VITRECTOMY CUTTER (November 4, 2003)
  • K030948 — VMATE MODEL VMM1000 (June 17, 2003)
  • K023939 — VELOCITY ADVANTAGE (April 17, 2003)

FDA data resources