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

RHEUMA-LEX(TM) SYST: RHEUMATOID FACTOR LATEX TEST

K Number: K915320 · Decision Dec 7, 1992
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
143
Applicant Total
44
Review Days
381

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Basic Information

Device Name
RHEUMA-LEX(TM) SYST: RHEUMATOID FACTOR LATEX TEST
K Number
K915320
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5775
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Trinity Laboratories, Inc.
Date Received
November 22, 1991
Decision Date
December 7, 1992
Product Code
DHR
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
DHR System, Test, Rheumatoid Factor

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K972160 CRP-LEX SYSTEM: C-REACTIVE PROTEIN ANTIGEN DETECTION IN SERUM: SLIDE AGGLUTNATION LATEX TEST
K970722 EYE TRAY
K965201 O.R. SCRUB PREP TRAY, STERILE, DISPOSABLE
K964921 BASIC BIOPSY TRAY. DISPOSABLE, STERILE
K953929 MID-STREAM COLLECTION SET-STERILE
K952058 STERILE V.A.D. (VASCULAR ACCESS DEVICES) ACCESS KIT, DISPOSABLE
K953070 WOUNDFOAM 4 X 4
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