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510(k) K060953

OCCULTECH FECAL OCCULT BLOOD RAPID TEST by Yd Diagnostics Corp. — Product Code KHE

K060953 is an FDA 510(k) premarket notification submitted by Yd Diagnostics Corp. for the device "OCCULTECH FECAL OCCULT BLOOD RAPID TEST". The FDA issued a decision of Substantially Equivalent on September 18, 2006. The device falls under product code KHE (Reagent, Occult Blood), a Class II device regulated under 21 CFR 864.6550. Yd Diagnostics Corp. has at least 3 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 18, 2006
Date Received
April 6, 2006
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Reagent, Occult Blood
Device Class
Class II
Regulation Number
864.6550
Review Panel
HE
Submission Type

Other clearances by Yd Diagnostics Corp.

  • K141874 — URISCAN OPTIMA (May 28, 2015)
  • K050801 — URISCAN OPTIMA II URINE ANALYZER (April 20, 2005)
  • K023027 — PREG-Q EARLY PREGNANCY TEST (December 16, 2002)

Other clearances for product code KHE

  • K173212 — Instant-view-PLUS immunochemical Fecal Occult Blood Test (February 15, 2018)
  • K170548 — InSure ONE (October 5, 2017)
  • K171484 — hema-screen SPECIFIC Gold (June 14, 2017)
  • K162333 — Wondfo One Step Fecal Occult Blood (FOB) Test (May 14, 2017)
  • K163554 — hema-screen ER XCEL Enhanced Readability Fecal Occult Blood Test (January 17, 2017)
  • K143325 — OC-Light S FIT (August 20, 2015)
  • K121397 — OSOM IFOB 25 TEST AND PATIENT COLLECTION KIT OSOM IFOB CONTROL KIT OSOM IFOB 50 (December 28, 2012)
  • K113506 — IND ONE STEP OCCULT BLOOD (FOB) TEST (December 19, 2012)
  • K110309 — FOB ONE STEP RAPID TEST (September 14, 2011)
  • K102664 — HEMA SCREEN ER (January 28, 2011)

FDA data resources