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

ARTIMICROBIAL REMOVAL DEVICE

K Number: K830372 · Decision Apr 8, 1983
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
3
Applicant Total
38
Review Days
63

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Basic Information

Device Name
ARTIMICROBIAL REMOVAL DEVICE
K Number
K830372
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2560
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Marion Laboratories, Inc.
Date Received
February 4, 1983
Decision Date
April 8, 1983
Product Code
LJF
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
LJF Device, Antimicrobial Drug Removal

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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
K870864 CULTURETTE BRAND CDT CLOSTRIDIUM DIFFICILE TEST
K863485 MODIFICATION OF CDT(TM) CLOSTRIDIUM TEST
K862123 BIOSPHERE ANAEROBIC ENVIRONMENTAL DEVICE
Search all 38 clearances from Marion Laboratories, Inc. →