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

KWIK STIK(TM) LYFO(TM) DISK MICROORGANISMS

K Number: K861022 · Decision Apr 4, 1986
Classifications
1
FEI Numbers
9
Registration Numbers
9
Same Product Code
11
Applicant Total
9
Review Days
17

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Basic Information

Device Name
KWIK STIK(TM) LYFO(TM) DISK MICROORGANISMS
K Number
K861022
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2480
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Micro-Bio-Logics
Date Received
March 18, 1986
Decision Date
April 4, 1986
Product Code
JTR
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
JTR Kit, Quality Control For Culture Media

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JTR), 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
K861312 LYFO-KWIK (TM) COAGULASE PLASMA
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