FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

RUBELLA IGG EIA TEST KIT

K Number: K853696 · Decision Jun 17, 1986
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
93
Applicant Total
17
Review Days
285

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Basic Information

Device Name
RUBELLA IGG EIA TEST KIT
K Number
K853696
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3510
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Labsystems, Inc.
Date Received
September 5, 1985
Decision Date
June 17, 1986
Product Code
LFX
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
LFX Enzyme Linked Immunoabsorbent Assay, Rubella

Similar 510(k) Clearances

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

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Other Clearances by Labsystems, Inc.

K Number Device Name
K923365 TILT/REDUCED SHEAR SEMI-RECLINE SEATING SYSTEM
K896474 RESUBMITTED FECATWIN SENSITIVE - FECA-EIA
K890154 MODIFIED LABYSYSTEMS' TOXOPLASMA GONDII IGG EIA
K890091 MODIFIED LABSYSTEMS' RUBELLA IGG EIA TEST KIT
K881243 RUBELLA IGG - EIA TEST KIT NUMBER 61 07 201
K873780 MODIFICATION RUBELLA IGM EIA TEST KIT
K873583 AUTO-EIA
K872252 MODIFIED TOXOPLASMA GONDII IGG EIA TEST KIT
K862705 CYTOMEGALOVIRUS IGG EIA TEST KIT
K862431 RUBELLA IGM EIA TEST KIT
Search all 17 clearances from Labsystems, Inc. →