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

ENTERO-TEST HP, MODEL #102-01

K Number: K983119 · Decision Mar 15, 1999
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
62
Applicant Total
30
Review Days
188

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Basic Information

Device Name
ENTERO-TEST HP, MODEL #102-01
K Number
K983119
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2900
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hdc Corp.
Date Received
September 8, 1998
Decision Date
March 15, 1999
Product Code
LIO
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
LIO Device, Specimen Collection

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