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

SELECT IUI

K Number: K954099 · Decision Nov 22, 1995
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
28
Applicant Total
6
Review Days
83

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Basic Information

Device Name
SELECT IUI
K Number
K954099
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.5250
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Select Medical Systems, Inc.
Date Received
August 31, 1995
Decision Date
November 22, 1995
Product Code
MFD
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
MFD Cannula, Intrauterine Insemination

Similar 510(k) Clearances

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

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Other Clearances by Select Medical Systems, Inc.

K Number Device Name
K012935 THECURVE, ITEM 507
K974819 SELECTCELLS(TM) MINI
K954097 SELECTCELLS STANDARD
K954102 SELECTMUCUS
K942922 SELECTA 20/60 CHEMISTRY ANALYZER