FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

WORLDWIDE MEDICAL TECHNOLOGIES NEEDLE GUIDE

K Number: K981470 · Decision Jun 19, 1998
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
175
Applicant Total
15
Review Days
57

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Basic Information

Device Name
WORLDWIDE MEDICAL TECHNOLOGIES NEEDLE GUIDE
K Number
K981470
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1710
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Worldwide Medical Technologies, LLC
Date Received
April 23, 1998
Decision Date
June 19, 1998
Product Code
IZH
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IZH System, X-Ray, Mammographic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (IZH), ordered by most recent decision date.

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Other Clearances by Worldwide Medical Technologies, LLC

K Number Device Name
K062214 BRACHYSCIENCES STRANDPORT
K023179 READI-STRAND, MODEL PSSTRAND
K022705 READI-STRAND, MODEL PSSTRAND
K022389 READI-LOAD SYSTEM, MODEL PSS 1820RL
K020641 SPIRITUS(TM) RESPIRATORY SYSTEM #SRS 001
K020337 READI-STRAND; MODEL PSSTRAND
K020867 BONE MARROW ASPIRATION NEEDLE, MODEL BMB1110J, BONE MARROW HARVEST NEEDLE, MODEL BMHN1104VX, & BONE MARROW BIOPSY NEEDL
K991344 WORLDWIDE MEDICAL TECHNOLOGIES SEEDING SPACERS
K981889 WORLDWIDE MEDICAL TECHNOLOGIES INTRODUCER NEEDLE
K982097 WORLDWIDE MEDICAL TECHNOLOGIES INTRACERVICAL BLOCK NEEDLE, MODEL TBD
Search all 15 clearances from Worldwide Medical Technologies, LLC →