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510(k) K926425

AMNIPERF(TM) by Raymart Development Co. — Product Code HGE

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 7, 1994
Date Received
December 23, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Amniotome
Device Class
Class I
Regulation Number
884.4530
Review Panel
OB
Submission Type

Other clearances for product code HGE

  • K951148 — OBSTI-HOOK (June 9, 1995)
  • K910518 — GLOVE-N-GEL AMNIOTOMY KIT (May 9, 1991)
  • K871087 — S.C.M.T. PERFORATOR (March 23, 1987)
  • K850758 — AMNIGLOVE & AMNICOT (April 15, 1985)
  • K834177 — H.R. JAKOBI SURG. INSTRUMENTS #4 30/31 (December 27, 1983)