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EUDAMED
FDA 510(k)
11
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52 devices found
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Manufacturer: The Prometheus Group
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Device · Manufacturer · Authorizations
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Status
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Class
Pathway MR-15
Prometheus Group Of New Hampshire Limited, The
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Pathway Ii Electromyograph
The Prometheus Group
·
,
FDA registration: United States
Class II
FDA 510(k)
K897132
Active
Cleared 18 Apr 1991
Active
510(k)
510(k)
II
Pathway Stm-10 Pelvic Floor Stimulator
The Prometheus Group
·
,
FDA registration: United States
Class II
FDA 510(k)
K030039
Active
Cleared 23 May 2003
Active
510(k)
510(k)
II
Pathway Cts 2000 Pelvic Floor Training System, Model Pathway Cts 2000
The Prometheus Group
·
,
FDA registration: United States
Class II
FDA 510(k)
K001515
Active
Cleared 31 Jul 2000
Active
510(k)
510(k)
II
Pathway Electromyograph Model Pathway Ii/Mr-10/Mr-15/Mr-20/Mr-25
The Prometheus Group
·
,
FDA registration: United States
Class II
FDA 510(k)
K960508
Active
Cleared 16 Jan 1997
Active
510(k)
510(k)
II
Pathway Vaginal Emg/Stim Perineometer Sensor, Pathway Anal Emg/Stim Perineometer Sensor
The Prometheus Group
·
,
FDA registration: United States
Class II
FDA 510(k)
K993976
Active
Cleared 22 Feb 2000
Active
510(k)
510(k)
II
Morpheus RealTime Ultrasound, Pathway RealTime Ultrasound, QuickScan Bladder Ultrasound
The Prometheus Group
·
,
FDA registration: United States
Class II
FDA 510(k)
K160792
Active
Cleared 15 Apr 2016
Active
510(k)
510(k)
II
Pathway Electromyograph
The Prometheus Group
·
,
FDA registration: United States
Class II
FDA 510(k)
K973537
Active
Cleared 17 Dec 1997
Active
510(k)
510(k)
II
Pathway CTS2000 Pelvic Floor Training System
The Prometheus Group
·
,
FDA registration: United States
Class II
FDA 510(k)
K023906
Active
Cleared 19 Feb 2003
Active
510(k)
510(k)
II
Pathway Vaginal/Rectal Perineometer Probe
The Prometheus Group
·
,
FDA registration: United States
Class II
FDA 510(k)
K974036
Active
Cleared 22 Dec 1997
Active
510(k)
510(k)
II
Pathway Electromyograph Model Tr-10 & Tr-20
The Prometheus Group
·
,
FDA registration: United States
Class II
FDA 510(k)
K960761
Active
Cleared 7 Aug 1996
Active
510(k)
510(k)
II
Synergy Plus
The Prometheus Group
·
,
FDA registration: United States
Class II
FDA 510(k)
K960762
Active
Cleared 13 Jun 1996
Active
510(k)
510(k)
II
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