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

LKB ULTROBACT (TM) PNEUMOCOCCUS KIT; 2321-110

K Number: K862848 · Decision Dec 18, 1986
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
8
Applicant Total
52
Review Days
142

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Basic Information

Device Name
LKB ULTROBACT (TM) PNEUMOCOCCUS KIT; 2321-110
K Number
K862848
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3740
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Lkb Instruments, Inc.
Date Received
July 29, 1986
Decision Date
December 18, 1986
Product Code
GWC
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
GWC Antisera, All Types, Streptococcus Pneumoniae

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Other Clearances by Lkb Instruments, Inc.

K Number Device Name
K874094 1205 BETAPLATE LIQUID SCINTILLATION COUNTER
K872955 DELFIA(TM) FERRITIN KIT
K871303 DELFIA(TM) THYROXINE (T4) KIT
K871599 DELFIA(TM) HIGE KIT
K871644 DELFIA (TM) HTSH KIT
K864452 DELFIA(TM) TRIIODOTHYRONINE (T3) KIT
K864733 LKB 2260 MACROTOME
K863422 DELFIA(TM) CORTISOL KIT
K861195 DELFIA DIGOXIN
K862044 DELFIA (TM) HCG KIT
Search all 52 clearances from Lkb Instruments, Inc. →