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

HYCOR HY.TEC/MANUAL RNP AUTO-ANTIBODY

K Number: K962727 · Decision Mar 7, 1997
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
179
Applicant Total
51
Review Days
249

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
HYCOR HY.TEC/MANUAL RNP AUTO-ANTIBODY
K Number
K962727
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Hycor Biomedical, Inc.
Date Received
July 1, 1996
Decision Date
March 7, 1997
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.

View all

Other Clearances by Hycor Biomedical, Inc.

K Number Device Name
K081217 HY-TEC SPECIFIC AND TOTAL IGE EIA SYSTEM
K080322 HY*TEC EXTENDED SPECIFIC IGE EIA, MCS ASSAY USING TECAN FREEDOM EVO RSP 200
K022944 AUTOSTAT II ANTI-B-2 GLYCOPROTEIN-I IGM ELISA
K022945 AUTOSTAT II ANTI-B-2 GLYCOPROTEIN I IGG ELISA
K965094 HYCOR ALLERGEN DISC
K962730 HYCOR HY.TEC/MANUAL DS-DNA AUTO-ANTIBODY
K962720 HYCOR HY.TEC/MANUAL SCL-70 AUTO-ANTIBODY
K962729 HYCOR HY.TEC/MANUAL RF AUTO-ANTIBODY
K962578 HYCOR HY.TEC/MANUAL SS-B AUTO-ANTIBODY
K962722 HYCOR HY.TEC/MANUAL SM AUTO-ANTIBODY
Search all 51 clearances from Hycor Biomedical, Inc. →