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510(k) K082056

ANORECTAL MANOMETRY SOFTWARE OPTION ARM-1 by Life-Tech, Inc. — Product Code FFX

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 7, 2008
Date Received
July 21, 2008
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Gastrointestinal Motility (Electrical)
Device Class
Class II
Regulation Number
876.1725
Review Panel
GU
Submission Type

Other clearances by Life-Tech, Inc.

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  • K102813 — EZONO 3000 (June 30, 2011)
  • K102007 — PROLONG, MODELS PL 18040TC, PL18050TGC, PL18100TGC, PL18150TGC, (December 22, 2010)
  • K093662 — ECHOBRIGHT (June 24, 2010)
  • K093485 — VESISCAN (March 16, 2010)
  • K082772 — STIMPRO, MODELS SP22050, SP20100, SPP19050, SPP19100, SPP19150, SPC19050, SPC191 (February 9, 2009)
  • K082923 — PRLONG, MODELS PL50, PL100, PL-40C, PL-50C, PL-100C, PL-150C, PLT-40C, PLT-50C, (October 24, 2008)
  • K081864 — PROLONG (September 25, 2008)
  • K073187 — PERIPHERAL NERVE BLOCK SUPPORT TRAY (April 22, 2008)

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