FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

WELLCOLEX E-COLI OI57 ZC60

K Number: K962028 · Decision Nov 1, 1996
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
11
Applicant Total
2
Review Days
162

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Basic Information

Device Name
WELLCOLEX E-COLI OI57 ZC60
K Number
K962028
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3255
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Murex Diagnostics, Inc.
Date Received
May 23, 1996
Decision Date
November 1, 1996
Product Code
GNA
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
GNA Antisera, All Types, Escherichia Coli

Similar 510(k) Clearances

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

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Other Clearances by Murex Diagnostics, Inc.

K Number Device Name
K954920 MUREX RUB-EX