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

CULTURETTE BRAND CDT CLOSTRIDIUM DIFFICILE TEST

K Number: K870864 · Decision Apr 14, 1987
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
41
Applicant Total
38
Review Days
42

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Basic Information

Device Name
CULTURETTE BRAND CDT CLOSTRIDIUM DIFFICILE TEST
K Number
K870864
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2660
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Marion Laboratories, Inc.
Date Received
March 3, 1987
Decision Date
April 14, 1987
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

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Other Clearances by Marion Laboratories, Inc.

K Number Device Name
K883391 POLYMER ADHESIVE BANDAGE
K875182 MODIFIED LABELING FOR TOXI-LAB THC SCREEN
K875181 MODIFIED LABELING FOR TOXI-LAB BROAD SPECTRUM
K874554 ENVICLUSIVE (TM)
K874551 ENVINET(TM)
K874552 ENVISAN PAD
K874553 ENVISAN PASTE
K863485 MODIFICATION OF CDT(TM) CLOSTRIDIUM TEST
K862123 BIOSPHERE ANAEROBIC ENVIRONMENTAL DEVICE
K853073 CULTURETTE BRAND 10-MINUTE GROUP A STREP I.D.
Search all 38 clearances from Marion Laboratories, Inc. →