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510(k) K051889

CAREVENT CA AND DRA by O-Two Medical Technologies, Inc. — Product Code BTL

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 30, 2005
Date Received
July 12, 2005
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ventilator, Emergency, Powered (Resuscitator)
Device Class
Class II
Regulation Number
868.5925
Review Panel
AN
Submission Type

Other clearances by O-Two Medical Technologies, Inc.

  • K173205 — Equinox Advantage (August 29, 2018)
  • K141595 — O-TWO E700,O-TWO E600,O-TWO E500 (March 16, 2015)
  • K113687 — EQUINOX RELIEVE (April 30, 2012)
  • K112546 — O_TWO CPAP SYSTEM (December 27, 2011)
  • K093862 — CAREVENT HANDHELD CPAP SYSTEM (May 6, 2010)
  • K081330 — CAREVENT PAR (PUBLIC ACCESS RESUSCITATOR) (March 6, 2009)
  • K051469 — CAREVENT ATV+ AND CAREVENT MRI (September 28, 2005)

Other clearances for product code BTL

  • K242769 — VentStar Resus heated (N) (MP17030); VentStar Autobreath heated (N) (MP17031) (April 4, 2025)
  • K221634 — Oxymag - Transport and Emergency Ventilator (May 24, 2023)
  • K202219 — VORTRAN GO2VENT with PEEP Valve (February 11, 2021)
  • K193191 — MEDUMAT Easy CPR, MEDUMAT Easy CPR with bag (November 20, 2020)
  • K182956 — Puffin Lite Infant Resuscitation System (January 18, 2019)
  • K173373 — SafeT T-Piece Resuscitator (November 16, 2018)
  • K161420 — MOVES SLC (June 6, 2017)
  • K162968 — VORTRAN GO2VENT (April 10, 2017)
  • K141595 — O-TWO E700,O-TWO E600,O-TWO E500 (March 16, 2015)
  • K142096 — T-PIECE RESUSCITATOR (October 17, 2014)