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510(k) K952085

DPD DEFIBRILLATOR by Medical Research Laboratories, Inc. — Product Code LDD

K952085 is an FDA 510(k) premarket notification submitted by Medical Research Laboratories, Inc. for the device "DPD DEFIBRILLATOR". The FDA issued a decision of ST on June 5, 1995. The device falls under product code LDD (Dc-Defibrillator, Low-Energy, (Including Paddles)), a Class II device regulated under 21 CFR 870.5300. Medical Research Laboratories, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
ST ()
Decision Date
June 5, 1995
Date Received
May 3, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Dc-Defibrillator, Low-Energy, (Including Paddles)
Device Class
Class II
Regulation Number
870.5300
Review Panel
CV
Submission Type

Other clearances by Medical Research Laboratories, Inc.

  • K021168 — JUMP START, MODEL 970300 (June 26, 2002)
  • K012766 — PORTABLE INTENSIVE CARE UNIT (January 23, 2002)
  • K012030 — PORTABLE INTENSIVE CARE UNIT (September 24, 2001)
  • K010207 — PORTABLE INSTENSIVE CARE UNIT (June 14, 2001)
  • K002232 — AEDEFIBRILLATOR (December 6, 2000)
  • K000712 — PORTABLE INTENSIVE CARE UNIT, MODEL PIC (April 27, 2000)
  • K983307 — MODIFICATION TO PORTABLE INTENSIVE CARE UNIT (November 20, 1998)
  • K974034 — PORTABLE INTENSIVE CARE UNIT (March 2, 1998)
  • K935922 — 360 SLX ADVISORY DEFIBRILLATOR (December 22, 1994)
  • K930548 — DPD DEFIBRILLATOR (June 25, 1993)

Other clearances for product code LDD

  • K203231 — Switched Internal Paddles (January 11, 2021)
  • K200849 — Tempus LS - Manual (July 24, 2020)
  • K182503 — Sterilizable Internal Defibrillation Paddles for use with LIFEPAK defibrillators (June 3, 2019)
  • K150349 — Rapid Hair Removal Pads (July 14, 2015)
  • K140502 — ZOLL E SERIES ALS (November 6, 2014)
  • K103651 — CARDIOMED (October 4, 2011)
  • K103783 — EURO DEFI PADS ADULT; EURO DEFI PADS ADULT RADIOTRANSPARENT: EURO DEFI PADS PEDI (June 16, 2011)
  • K103334 — CARDIO MED (January 18, 2011)
  • K103159 — CARDIO MED MODEL A102, H104, O101, P103, AND Z100 (January 11, 2011)
  • K102468 — ZOLL PROPAQ MD (September 30, 2010)

FDA data resources