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510(k) K002321

PAIN CARE 2000L by Breg, Inc. — Product Code MEB

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 14, 2000
Date Received
July 31, 2000
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pump, Infusion, Elastomeric
Device Class
Class II
Regulation Number
880.5725
Review Panel
HO
Submission Type

Other clearances by Breg, Inc.

  • K183702 — Polar Care Wave (March 1, 2019)
  • K070402 — MODIFICATION TO POLAR CARE 500 (March 29, 2007)
  • K041714 — E-PAIN CARE (October 1, 2004)
  • K020988 — PAIN CARE 4200 (April 4, 2002)
  • K013928 — PAIN CARE 3200 (December 3, 2001)
  • K003611 — PAIN CARE MULTI-PORT CATHETER, MODEL 2000L (December 13, 2000)
  • K002073 — PAIN CARE 3000 (September 19, 2000)
  • K983454 — PAIN CARE 2000 (December 16, 1998)
  • K963596 — POLAR CARE 300 (December 4, 1996)
  • K961855 — POLAR CARE (MODEL 500/50000) (August 9, 1996)

Other clearances for product code MEB

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  • K181360 — ON-Q* Pump with Bolus (March 22, 2019)
  • K151650 — SMARTez elastomeric infusion pump (April 4, 2016)
  • K131249 — ON-Q PAINBUSTER, ON-Q C-BLOC, HOMEPUMP ECLIPSE, HOMEPUMP C-SERIES (February 3, 2014)
  • K131247 — MULTIBOLUS II DISPOSABLE PAIN MANAGEMENT SYSTEM (August 14, 2013)
  • K090300 — MODIFICATION TO AUTOFUSER (April 30, 2009)
  • K081905 — ACCUFLOW AND ACCUFLUX ELASTOMERIC INFUSION PUMP (July 15, 2008)
  • K071532 — ALPHA INFUSION PUMP, MODEL A200, A450 (February 19, 2008)
  • K072921 — DISPOSABLE INFUSION PUMP KIT, GO PUMP RAPID RECOVERY SYSTEM (November 26, 2007)