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17 devices found
·
sorted by relevance
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Manufacturer: Imex, LLC
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Device · Manufacturer · Authorizations
Verified
Status
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Registry
Class
Imex 5MHZ DOPPLER PROBE, PD2 T500
Imex, LLC
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Imex ELITE 3MHZ OB PROBE N300
Imex, LLC
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Imex 3MHZ DOPPLER PROBE, PD2 T300
Imex, LLC
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Imex 8MHZ DOPPLER PROBE, PD2 T800
Imex, LLC
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Imex 2MHZ Doppler Probe PD2 T200
Imex, LLC
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Imex DOPPLER PROBE, 2MHZ, H2O PROOF PDII WP20
Imex, LLC
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Imex Elite 200 Doppler
Imex, LLC
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Imex Elite 100 Doppler
Imex, LLC
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Imex Pocket Dop II Doppler System
Imex, LLC
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Imex Elite 200R Doppler
Imex, LLC
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Imex CT+ Doppler
Imex, LLC
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Imex Elite 100R Doppler
Imex, LLC
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Imex ELITE 2MHZ WATERPROOF PROBE V2 NW20
Imex, LLC
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Imex ELITE 8MHZ VASCULAR PROBE N800
Imex, LLC
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Imex ELITE 2MHZ OB PROBE N200
Imex, LLC
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Elite 5 MHz Vascular Probe N500
Imex, LLC
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Mentor Mds
Imex
·
,
FDA registration: United States
Class II
FDA 510(k)
K885155
Active
Cleared 14 Mar 1989
Active
510(k)
510(k)
II
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