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510(k) K872312

MODEL 3000 OPHTHALMIC SURGICAL SYSTEM by Allergan Humphrey — Product Code HQE

K872312 is an FDA 510(k) premarket notification submitted by Allergan Humphrey for the device "MODEL 3000 OPHTHALMIC SURGICAL SYSTEM". The FDA issued a decision of Substantially Equivalent on July 15, 1987. The device falls under product code HQE (Instrument, Vitreous Aspiration And Cutting, Ac-Powered), a Class II device regulated under 21 CFR 886.4150. Allergan Humphrey has at least 2 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 15, 1987
Date Received
April 14, 1987
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 Allergan Humphrey

  • K902582 — ALLERGAN HUMPHREY A/B SCAN , MODEL 835 (August 14, 1990)
  • K871611 — ALLERGAN HUMPHREY AUTO-REFRACTOR, MODELS 525 & 540 (May 18, 1987)

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