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

CDT CYTOTOXI TEST

K Number: K883560 · Decision Oct 25, 1988
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
41
Applicant Total
19
Review Days
67

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Basic Information

Device Name
CDT CYTOTOXI TEST
K Number
K883560
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2660
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Advanced Clinical Diagnostics
Date Received
August 19, 1988
Decision Date
October 25, 1988
Product Code
LLH
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
LLH Reagents, Clostridium Difficile Toxin

Similar 510(k) Clearances

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

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Other Clearances by Advanced Clinical Diagnostics

K Number Device Name
K936171 TRANSFORMED PRIMARY HUMAN EMBRYONAL KIDNEY
K936172 RHESUS MONKEY KIDNEY CELLS (LLC-MK2)
K936169 RHESUS MONKEY KIDNEY CELLS
K934973 HELA-229/HELA CELLS
K934934 RABBIT KIDNEY CELLS - R.K.C.
K935766 PRIMARY AFRICAN GREEN MONKEY KIDNEY CELLS
K935336 CYNOMOLOGUS MONKEY KIDNEY CELLS
K934241 MCCOY CULTURE CELLS-MCCOY
K934243 HUMAN EPIDERMAL CARCINOMA LARYNX CELLS-HEP-2
K934246 LUNG DIPLOID HUMAN CELLS-WI-38
Search all 19 clearances from Advanced Clinical Diagnostics →