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510(k) K884095

SCISSORS, WIRE CUTTING by Magnatrade Corp. — Product Code LRW

K884095 is an FDA 510(k) premarket notification submitted by Magnatrade Corp. for the device "SCISSORS, WIRE CUTTING". The FDA issued a decision of Substantially Equivalent on October 19, 1988. The device falls under product code LRW (Scissors, General, Surgical), a Class I device regulated under 21 CFR 878.4800.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 19, 1988
Date Received
September 28, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Scissors, General, Surgical
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type

Other clearances for product code LRW

  • K911158 — MICRO SCISSORS, 5MM CURVE MICRO SCISSORS, 5MM (March 29, 1991)
  • K902828 — SUTURE REMOVAL TRAY (August 8, 1990)
  • K900957 — GS-2100 HOOK SUTURE SCISSOR, 5MM (April 18, 1990)
  • K900950 — GS-2000 MICRO SCISSOR, CURVED LEFT, 5MM (April 18, 1990)
  • K892823 — PLASTER CUTTING SCISSORS (May 25, 1989)
  • K891889 — OLIVECORONA SCISSORS (April 12, 1989)
  • K891886 — SCISSORS, VARIOUS TYPES (April 12, 1989)
  • K891200 — RIBBON TYPE SCISSORS: TENOTOMY,IRIS,EYE,STRABISMUS (April 6, 1989)
  • K891203 — SCISSORS: THOREK, JORGENSEN, FINOCHIETTO (April 6, 1989)
  • K890170 — SCISSORS (February 3, 1989)

FDA data resources