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

LKB-WALLAC 1230 ARCUS FLUOROMETER

K Number: K851984 · Decision May 24, 1985
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
37
Applicant Total
52
Review Days
17

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
LKB-WALLAC 1230 ARCUS FLUOROMETER
K Number
K851984
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2560
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Lkb Instruments, Inc.
Date Received
May 7, 1985
Decision Date
May 24, 1985
Product Code
KHO
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
KHO Fluorometer, For Clinical Use

Similar 510(k) Clearances

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

View all

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
K862848 LKB ULTROBACT (TM) PNEUMOCOCCUS KIT; 2321-110
K863422 DELFIA(TM) CORTISOL KIT
K861195 DELFIA DIGOXIN
Search all 52 clearances from Lkb Instruments, Inc. →