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

ANORECTAL MANOMETRY SOFTWARE OPTION ARM-1

K Number: K082056 · Decision Nov 7, 2008
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
68
Applicant Total
14
Review Days
109

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Basic Information

Device Name
ANORECTAL MANOMETRY SOFTWARE OPTION ARM-1
K Number
K082056
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1725
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Life-Tech, Inc.
Date Received
July 21, 2008
Decision Date
November 7, 2008
Product Code
FFX
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FFX System, Gastrointestinal Motility (Electrical)

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Other Clearances by Life-Tech, Inc.

K Number Device Name
K120234 EZONO 3000
K111355 ECHOBRIGHT
K102813 EZONO 3000
K102007 PROLONG, MODELS PL 18040TC, PL18050TGC, PL18100TGC, PL18150TGC,
K093662 ECHOBRIGHT
K093485 VESISCAN
K082772 STIMPRO, MODELS SP22050, SP20100, SPP19050, SPP19100, SPP19150, SPC19050, SPC19100, SPC19150, SPC18050,SPC18100,SPC18150
K082923 PRLONG, MODELS PL50, PL100, PL-40C, PL-50C, PL-100C, PL-150C, PLT-40C, PLT-50C, PLT-100C, PLT-150C
K081864 PROLONG
K073187 PERIPHERAL NERVE BLOCK SUPPORT TRAY
Search all 14 clearances from Life-Tech, Inc. →