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510(k) K981071

ML MICROKERATOME by Med-Logics, Inc. — Product Code HNO

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 23, 1998
Date Received
March 24, 1998
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Keratome, Ac-Powered
Device Class
Class I
Regulation Number
886.4370
Review Panel
OP
Submission Type

Other clearances by Med-Logics, Inc.

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  • K022716 — MED-LOGICS MICROKERATOME BLADE, MODEL 7020CLB (October 11, 2002)
  • K010872 — ML BLADE, MODEL ML7030 (June 22, 2001)
  • K010353 — MED-LOGICS DISPOSABLE ALK TUBING (April 27, 2001)
  • K002515 — MEDLOGICS ML 4000, MODEL 4000 (February 22, 2001)
  • K002279 — ML EYE SPEAR, MODEL ML 27 ES (August 18, 2000)
  • K983448 — ML UNIVERSAL TUBING (December 18, 1998)
  • K972522 — ML-DISPOSABLE PAK (September 30, 1997)
  • K971173 — ML DISPOSABLE ALK TUBING (May 22, 1997)

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  • K043183 — EPI-K (March 25, 2005)
  • K043150 — AMADEUS II EPIKERATOME (January 31, 2005)
  • K042083 — MODIFICATION TO VISITOME 20-10 MICROKERATOME (November 16, 2004)