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510(k) K051438

VANGUARD REPROCESSED COMPRESSION GARMENTS (HILL-ROM) by Alliance Medical, Inc. — Product Code JOW

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 4, 2006
Date Received
June 1, 2005
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Sleeve, Limb, Compressible
Device Class
Class II
Regulation Number
870.5800
Review Panel
CV
Submission Type

Other clearances by Alliance Medical, Inc.

  • K060648 — REPROCESSED PHACOEMULSIFICATION TIPS (March 19, 2007)
  • K061045 — REPROCESSED ELECTROPHYSIOLOGY CATHETERS (August 31, 2006)
  • K060049 — REPROCESSED COMPRESSION SLEEVES (February 24, 2006)
  • K060091 — ALLIANCE MEDICAL CORPORATION REPROCESSED COMPRESSION SLEEVES (February 17, 2006)
  • K053316 — REPROCESSED COMPRESSION SLEEVES (February 13, 2006)
  • K052918 — REPROCESSED EXTERNAL FIXATION DEVICES (January 27, 2006)
  • K052414 — REPROCESSED ELECTROPHYSIOLOGY CATHETER (November 16, 2005)
  • K052603 — REPROCESSED DAIG LIVEWIRE ELECTROPHYSIOLOGY CATHETERS (November 16, 2005)
  • K050518 — REPROCESSED PHACOEMUISIFICATION TIPS (September 23, 2005)
  • K052062 — ALLIANCE MEDICAL CORPORATION REPROCESSED EXTERNAL FIXATION DEVICES (August 25, 2005)

Other clearances for product code JOW

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  • K251466 — VenAir, Sequential Compression System (9P-089000); VenAir, Sequential Compressio (October 28, 2025)
  • K251446 — PlasmaFlow X Compression Sleeve Device (XPF0001) (September 17, 2025)
  • K251086 — PnueAira (PNCU-01) (August 18, 2025)
  • K250817 — Coretech Compression System (Coretech RHB3003) (August 8, 2025)
  • K241096 — Venera 608 Deep Vein Thrombosis (DVT) Prevention System (January 15, 2025)
  • K240499 — ARTAIRA Arterial Compression Device (AACD01) (October 11, 2024)
  • K241746 — UMED REPROCESSED AIRCAST VENAFLOW FOOT CUFF; UMED REPROCESSED KENDALL SCD EXPRES (October 4, 2024)