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

HISTONE REACTIVE ANA

K Number: K883232 · Decision Sep 7, 1988
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
179
Applicant Total
11
Review Days
37

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Basic Information

Device Name
HISTONE REACTIVE ANA
K Number
K883232
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Val Tech Diagnostics, Inc.
Date Received
August 1, 1988
Decision Date
September 7, 1988
Product Code
LLL
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
LLL Extractable Antinuclear Antibody, Antigen And Control

Similar 510(k) Clearances

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

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Other Clearances by Val Tech Diagnostics, Inc.

K Number Device Name
K883570 HISTO-CHECK FUNGAL CONTROL SLIDES
K883571 HISTO-CHECK PARASITIC CONTROL SLIDES
K883569 HISTO-CHECK GRAM NEGATIVE SLIDES
K883568 HISTO-CHECK ACID FAST SLIDES
K883567 HISTO-CHECK LEGIONELLA CONTROL SLIDES
K883684 HERPES VIRUS CONTROL SLIDES
K883208 HISTO-CHECK SLIDES
K871395 DUAL SUBSTRATE ANA
K864668 ANA TEST KIT
K870732 RAT LIVER NUCLEI TEST SYSTEM
Search all 11 clearances from Val Tech Diagnostics, Inc. →