FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

PROSTATE SEEDING NEEDLE

K Number: K973184 · Decision Nov 21, 1997
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
35
Applicant Total
18
Review Days
88

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Basic Information

Device Name
PROSTATE SEEDING NEEDLE
K Number
K973184
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.5650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Promex, Inc.
Date Received
August 25, 1997
Decision Date
November 21, 1997
Product Code
IWJ
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
IWJ System, Applicator, Radionuclide, Manual

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Other Clearances by Promex, Inc.

K Number Device Name
K023450 BIOPSY SITE TISSUE MARKER DEVICE
K022634 CO-AXIAL INTRODUCER NEEDLE
K010400 VACUUM ASSISTED CORE BIOPSY DEVICE
K011270 AUTOMATED CORE BIOPSY DEVICE
K001132 BONE BIOPSY NEEDLE
K994272 AUTOMATED CORE BIOPSY DEVICE
K993435 MANUAL BONE MARROW BIOPSY DEVICE
K972865 PROMEX ENT TISSUE REMOVAL SYSTEM
K961078 AUTOMATED VITRECTOMY DEVICE
K960023 KIRSHNER WIRES (K-WIRE) & STEINMANN PINS
Search all 18 clearances from Promex, Inc. →