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510(k) K851047

PLASTIC TUBE EXTENTION SET by Medovations, Inc.

K851047 is an FDA 510(k) premarket notification submitted by Medovations, Inc. for the device "PLASTIC TUBE EXTENTION SET". The FDA issued a decision of Substantially Equivalent on Apr 25, 1985. Medovations, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
Apr 25, 1985
Date Received
Mar 14, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Medovations, Inc.

  • K142068 — BULLDOG BIOPSY VALVE, OLYMPUS AND FUJINON;PENTAX COMPATIBLE;DISPOSABLE RRIGATING (Mar 10, 2015)
  • K002363 — MEDOVATIONS ESOPHAGEAL DILATOR (Nov 1, 2000)
  • K972119 — MALONEY BOUGE (1210-XX)/HURST BOUGIE (1212-XX) (Feb 2, 1998)
  • K924646 — OVER THE GUIDEWIRE DILATATION SYSTEM (Dec 5, 1994)
  • K913678 — TROCAR CATHETER (Dec 16, 1991)
  • K905478 — YANKAUER SUCTION DEVICE (Dec 19, 1990)
  • K874309 — URETHAL CATHETER (Dec 7, 1987)
  • K864963 — STOMACH EVACULATOR - EWALD STYLE (Oct 14, 1987)
  • K864962 — OBERTO MOUTH PROP (Feb 19, 1987)
  • K864964 — 5 - IN - 1 CONNECTOR (Jan 20, 1987)

FDA data resources