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

MINK LUNG

K Number: K852395 · Decision Jul 12, 1985
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
169
Applicant Total
25
Review Days
36

Basic Information

Device Name
MINK LUNG
K Number
K852395
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.2280
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
VIROMED LABORATORIES, INC.
Date Received
June 6, 1985
Decision Date
July 12, 1985
Product Code
KIR
Advisory Committee
Hematology
Review Advisory Committee
PA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KIR Cells, Animal And Human, Cultured

Similar 510(k) Clearances

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Other Clearances by VIROMED LABORATORIES, INC.

K Number Device Name
K951461 NCI-H292 CELL CULTURE
K951440 LLC-MK2 (MONKEY KIDNEY, MACACA MULATA) CELL CULTURE
K871613 BUFFALO GREEN MONKEY KIDNEY CELLS
K862555 HUMAN EPITHELOID CERVIX CARCINOMA CELLS (HELA)
K861373 HUMAN LUNG CARCINOMA CELLS (A549)
K853695 RESPIRATORY SYNCYTIAL VIRUS ID REAGENT
K852394 MDCK
K852396 HEK
K843250 BHK-21
K843251 RD CELLS
Search all 25 clearances from VIROMED LABORATORIES, INC. →