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510(k) K872919

OMNI-TRACT CORRAL RETRACTOR by Minnesota Scientific, Inc. — Product Code GAD

K872919 is an FDA 510(k) premarket notification submitted by Minnesota Scientific, Inc. for the device "OMNI-TRACT CORRAL RETRACTOR". The FDA issued a decision of Substantially Equivalent on August 11, 1987. The device falls under product code GAD (Retractor), a Class I device regulated under 21 CFR 878.4800. Minnesota Scientific, Inc. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 11, 1987
Date Received
July 27, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Retractor
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type

Other clearances by Minnesota Scientific, Inc.

  • K853948 — MINNESOTA SCIENTIFIC, INC. OMNI-BEAM (October 16, 1985)
  • K853947 — OMNI-TRACT CHEST WALL & LUNA RETRACTOR (October 16, 1985)
  • K842762 — OMNI-TRACT SURGICAL RETRACTOR SYS (August 17, 1984)
  • K810282 — OPERATING TABLE ACCESSORY CLAMP (February 26, 1981)

Other clearances for product code GAD

  • K152538 — JRP Wound Spreader (April 13, 2016)
  • K151104 — OTELO LL (January 6, 2016)
  • K132645 — THORATRAK MICS RETRACTOR SYSTEM, RACK, BLADES (October 4, 2013)
  • K071775 — DASH (August 7, 2007)
  • K050256 — APPLE MEDICAL/OB MOBIUS ELASTIC RETRACTOR (April 26, 2005)
  • K043602 — QUADRANT RETRACTOR SYSTEM (February 23, 2005)
  • K001339 — MRI FASTSYSTEM RETRACTOR SYSTEM (May 17, 2000)
  • K980588 — CLARUS ENDOSCOPIC DISCECTOMY SYSTEM SITETRAC MODEL 6000 (August 18, 1998)
  • K963006 — SCION SAPHENOUS VEIN HARVESTING SYSTEM (September 20, 1996)
  • K943875 — VILLALTA RETRACTOR (November 9, 1994)

FDA data resources