THE PROMETHEUS GROUP

FDA Registration(s)#

Registration, FEI, Name table
Registration	FEI	Name	Status	Initial importer	Expiration year	Address
1224842	1000513601	THE PROMETHEUS GROUP	1	N	2026-01-01	1 WASHINGTON ST., SUITE 3171 DOVER NH US 03820

Registration key, Listing key, Premarket submission table
Registration key	Listing key	Premarket submission	Device	Product code	Decision date
16001	1780912827	K993976	PATHWAY VAGINAL EMG/STIM PERINEOMETER SENSOR, PATHWAY ANAL EMG/STIM PERINEOMETER SENSOR	KPI	2000-02-22
16001	1941549226	K974036	PATHWAY VAGINAL/RECTAL PERINEOMETER PROBE	HIR	1997-12-22
16001	1062653040	K973537	PATHWAY ELECTROMYOGRAPH	HCC	1997-12-17
16001	1254281591	K960762	SYNERGY PLUS	HCC	1996-06-13
16001	1408584769	K960508	PATHWAY ELECTROMYOGRAPH MODEL PATHWAY II/MR-10/MR-15/MR-20/MR-25	HIR	1997-01-16
16001	1959316229	K160792	Morpheus RealTime Ultrasound, Pathway RealTime Ultrasound, QuickScan Bladder Ultrasound	IYO	2016-04-15
16001	1277437831	K030039	PATHWAY STM-10 PELVIC FLOOR STIMULATOR	KPI	2003-05-23
16001	1104037331	K023906	PATHWAY CTS2000 PELVIC FLOOR TRAINING SYSTEM	KPI	2003-02-19
16001	1152989973
16001	1631256208
16001	2045848039