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510(k) K810017

MICROSURG CAUTERY by Medical Products Development, Inc. — Product Code HQO

K810017 is an FDA 510(k) premarket notification submitted by Medical Products Development, Inc. for the device "MICROSURG CAUTERY". The FDA issued a decision of SESP on January 5, 1981. The device falls under product code HQO (Unit, Cautery, Thermal, Ac-Powered), a Class II device regulated under 21 CFR 886.4115. Medical Products Development, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESP ()
Decision Date
January 5, 1981
Date Received
January 5, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Unit, Cautery, Thermal, Ac-Powered
Device Class
Class II
Regulation Number
886.4115
Review Panel
OP
Submission Type

Other clearances by Medical Products Development, Inc.

  • K810016 — REPLACABLE BATTERY PERFECTEMP CAUTERY (April 23, 1981)
  • K810013 — MULTIPERFECTEMP CAUTERY (April 23, 1981)
  • K810012 — MULTIMICRO SURGICAL CAUTERY (April 23, 1981)
  • K803067 — SURG-FLEX 10 LIGHT (February 26, 1981)
  • K810015 — MULTIHI-TEMP CAUTERY (February 12, 1981)
  • K810014 — REPLACABLE BATTERY HI-TEMP CAUTERY (February 12, 1981)
  • K802942 — HITEMP. TM 2 LOOPTIP CAUTERY (February 4, 1981)
  • K810019 — SURG-FLEX 15 SURGICAL LIGHT (January 23, 1981)
  • K810018 — SURG-FLEX 5 SURGICAL LIGHT (January 23, 1981)
  • K802330 — HI-TEMP LOOPTIP SURGICAL CAUTERY (November 12, 1980)

Other clearances for product code HQO

  • K070871 — STARION UNIVERSAL POWER SUPPLY (April 13, 2007)
  • K043155 — STARION UNIVERSAL POWER SUPPLY (UPS) (December 9, 2004)
  • K002341 — THERMAL CAUTERY UNIT, MODEL 150 (October 23, 2000)
  • K000893 — AC POWERED THERMAL CAUTERY UNIT (June 14, 2000)
  • K971538 — MENTOR GEMINI HEMOSTATIC ERASER (July 14, 1997)
  • K962135 — D.O.R.C. MICRODIATHERMY SYSTEM (August 29, 1996)
  • K943031 — BIPOLAR ELECTROSURGICAL PENCIL (September 23, 1994)
  • K900913 — ADLER DISPOSABLE BIPOLAR CORD (April 4, 1990)
  • K874367 — VARIOUS CARDIAC CRYOPROBES HAVING DIA. & COS. DIFF (January 4, 1988)
  • K852075 — SITE-MALIS BIPOLAR COAGULATOR MODULE (August 20, 1985)

FDA data resources