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510(k) K883975

DISP. 20 GAUGE SITE FIBER OPTIC CABLE & ILLUMI. by Site Microsurgical Systems, Inc. — Product Code HQE

K883975 is an FDA 510(k) premarket notification submitted by Site Microsurgical Systems, Inc. for the device "DISP. 20 GAUGE SITE FIBER OPTIC CABLE & ILLUMI.". The FDA issued a decision of Substantially Equivalent on October 25, 1988. The device falls under product code HQE (Instrument, Vitreous Aspiration And Cutting, Ac-Powered), a Class II device regulated under 21 CFR 886.4150. Site Microsurgical Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 25, 1988
Date Received
September 20, 1988
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 Site Microsurgical Systems, Inc.

  • K925828 — MODIFIED SITE TXR SYSTEMS (February 16, 1994)
  • K925921 — MODIFIED SITE DISPOSABLE DIAPHRAGM CASSETTE (December 6, 1993)
  • K931866 — SITE'S CD II PHACOEMULSIFICATION HANDPIECE (November 12, 1993)
  • K921135 — IOLAB POWER I.V. POLE (June 3, 1992)
  • K920582 — 180 TIP, 1/A HANDPIECE .3MM END OPENING FOR OPHT. (May 8, 1992)
  • K912902 — PHACOEMULSIFICATION SYSTEM FOR OPHTHALMIC USE (December 17, 1991)
  • K912739 — SITE 90 TIP, I/A HANDPIECE .3MM SIDE OPEN/OPTH USE (August 28, 1991)
  • K910980 — SITE 20 GAUGE REUSABLE FIBER OPTIC CABLE (May 22, 1991)
  • K905620 — MODIFIED SITE PERISTALTIC FOOTSWITCH (February 27, 1991)
  • K904151 — SITE 19 GAUGE ULTRASONIC I/A PHACO NEEDLE (December 5, 1990)

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