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

LYFO-KWIK (TM) COAGULASE PLASMA

K Number: K861312 · Decision Apr 18, 1986
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
11
Applicant Total
9
Review Days
10

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Basic Information

Device Name
LYFO-KWIK (TM) COAGULASE PLASMA
K Number
K861312
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2160
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Micro-Bio-Logics
Date Received
April 8, 1986
Decision Date
April 18, 1986
Product Code
JTL
Advisory Committee
Microbiology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
JTL Plasma, Coagulase, Human, Horse And Rabbit

Similar 510(k) Clearances

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

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Other Clearances by Micro-Bio-Logics

K Number Device Name
K870731 LYFO KWIK(TM) RUS KIT
K861022 KWIK STIK(TM) LYFO(TM) DISK MICROORGANISMS
K855172 KWI (TM) G-CO/TWO
K855198 INDI KWIK (TM) CO/TWO KIT
K852998 NEISSERIA - KWIK PLUS
K851978 LYFO-KWIK OMI KIT
K844014 ONO/CO-TWO (TM) SYSTEMS
K842129 LYFO-DISK MICROORGANISMS