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510(k) K112998

AUTOPULSE RESUSCITATION SYSTEM MODEL 1000 by Zoll Circulation — Product Code DRM

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 15, 2012
Date Received
October 7, 2011
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Compressor, Cardiac, External
Device Class
Class II
Regulation Number
870.5200
Review Panel
CV
Submission Type

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Other clearances for product code DRM

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  • K161768 — LUCAS 3 Chest Compression System (November 9, 2016)
  • K153628 — ROSC-U Mini Chest Compressor (RMCC) (January 30, 2016)
  • K141809 — RMU-1000 AUTOMATED CHEST COMPRESSION SYSTEM (October 27, 2014)
  • K102068 — MINIATURIZE CHEST COMPRESSOR (MCC) (November 16, 2010)
  • K090422 — LUCAS 2 (June 17, 2009)
  • K072527 — AUTOPULSE RESUSCITATION SYSTEM, MODEL 100 (March 19, 2008)
  • K073079 — THUMPER, MODEL: 1008 (February 14, 2008)