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

HEMA SCREEN SPECIFIC IFOBT

K Number: K060463 · Decision Jun 6, 2006
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
96
Applicant Total
14
Review Days
104

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
HEMA SCREEN SPECIFIC IFOBT
K Number
K060463
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.6550
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Immunostics Inc.,
Date Received
February 22, 2006
Decision Date
June 6, 2006
Product Code
KHE
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
KHE Reagent, Occult Blood

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KHE), ordered by most recent decision date.

View all

Other Clearances by Immunostics Inc.,

K Number Device Name
K221817 ALFIS Vitamin D, ALFIS-3 Analyzer
K182298 hemochroma PLUS System
K163465 hemochroma PLUS System
K163225 AFIAS iFOB with AFIAS-50
K171484 hema-screen SPECIFIC Gold
K163554 hema-screen ER XCEL Enhanced Readability Fecal Occult Blood Test
K102664 HEMA SCREEN ER
K041728 HCG DETECTOR COMBI, HCG DETECTOR STIX, HCG DETECTOR CASSETTE
K031490 RUBELLACOL
K992759 COLON ALERT TEST
Search all 14 clearances from Immunostics Inc., →