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510(k) K020337

READI-STRAND; MODEL PSSTRAND by Worldwide Medical Technologies, LLC — Product Code KXK

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 29, 2002
Date Received
February 1, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Source, Brachytherapy, Radionuclide
Device Class
Class II
Regulation Number
892.5730
Review Panel
RA
Submission Type

Other clearances by Worldwide Medical Technologies, LLC

  • K062214 — BRACHYSCIENCES STRANDPORT (March 1, 2007)
  • K023179 — READI-STRAND, MODEL PSSTRAND (July 2, 2003)
  • K022705 — READI-STRAND, MODEL PSSTRAND (June 9, 2003)
  • K022389 — READI-LOAD SYSTEM, MODEL PSS 1820RL (May 6, 2003)
  • K020641 — SPIRITUS(TM) RESPIRATORY SYSTEM #SRS 001 (October 29, 2002)
  • K020867 — BONE MARROW ASPIRATION NEEDLE, MODEL BMB1110J, BONE MARROW HARVEST NEEDLE, MODEL (May 20, 2002)
  • K991344 — WORLDWIDE MEDICAL TECHNOLOGIES SEEDING SPACERS (November 5, 1999)
  • K981889 — WORLDWIDE MEDICAL TECHNOLOGIES INTRODUCER NEEDLE (July 31, 1998)
  • K982097 — WORLDWIDE MEDICAL TECHNOLOGIES INTRACERVICAL BLOCK NEEDLE, MODEL TBD (June 25, 1998)
  • K981470 — WORLDWIDE MEDICAL TECHNOLOGIES NEEDLE GUIDE (June 19, 1998)

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