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

XPECT CRYPTOSPORIDIUM LATERAL FLOW ASSAY, MODEL 2451020

K Number: K031965 · Decision Nov 14, 2003
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
14
Applicant Total
17
Review Days
141

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Basic Information

Device Name
XPECT CRYPTOSPORIDIUM LATERAL FLOW ASSAY, MODEL 2451020
K Number
K031965
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3220
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Remel, Inc.
Date Received
June 26, 2003
Decision Date
November 14, 2003
Product Code
MHJ
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
MHJ Cryptosporidium Spp.

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Other Clearances by Remel, Inc.

K Number Device Name
K162620 Remel Spectra ESBL
K131804 REMEL XPECT FLU A&B
K092407 REMEL SPECTRA MRSA
K072827 RPMI 1640 AGAR W/MOPS AND 2% GLUCOSE
K041951 XPECT CLOSTRIDIUM DIFFICILE TOXIN A/B
K033479 PROSPECT CLOSTRIDIUM DIFFICILE TOXIN A/B MICROPLATE ASSAY
K031942 XPECT GIARDIA LATERAL FLOW ASSAY, MODEL 2450020
K031834 XPECT GIARDIA/CRYPTOSPORIDIUM LATERAL FLOW ASSAY
K031565 XPECT INFLUENZA A/B
K981391 PAR-ONE
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