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510(k) K852180

SURGIDYNES VARIDYNE 350-2I & 350-2C CORDLESS ELEC. by Surgidyne, Inc.

K852180 is an FDA 510(k) premarket notification submitted by Surgidyne, Inc. for the device "SURGIDYNES VARIDYNE 350-2I & 350-2C CORDLESS ELEC.". The FDA issued a decision of SN on July 1, 1985. Surgidyne, Inc. has at least 5 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
July 1, 1985
Date Received
May 20, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Surgidyne, Inc.

  • K892334 — LEONARD TUBE (May 31, 1989)
  • K883582 — VARIDYNE MODEL 250 SUCTION DRAINAGE SYSTEM (October 3, 1988)
  • K864822 — VARIDYNE 550, MODELS 12E,12M,24E & 24M SUCTION SYS (January 15, 1987)
  • K860030 — SURGIDYNE VARIDYNE, MODEL 140-2I & MODEL 140-2ID (February 12, 1986)
  • K850634 — SURGIDYNE SURGIFLO C.W.S. DRAIN PRODUCTS (June 28, 1985)

FDA data resources