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

IRON/TOTAL IRON BINDING CAPACITY

K Number: K901561 · Decision May 17, 1990
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
66
Applicant Total
36
Review Days
44

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
IRON/TOTAL IRON BINDING CAPACITY
K Number
K901561
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1410
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Tech-Co, Inc.
Date Received
April 3, 1990
Decision Date
May 17, 1990
Product Code
JIY
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
JIY Photometric Method, Iron (Non-Heme)

Similar 510(k) Clearances

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

View all

Other Clearances by Tech-Co, Inc.

K Number Device Name
K921968 IN VITRO DIAGNOSTIC REAGENT SET, INDIR. PREG. TEST
K923376 VISUAL HCG PREGNANCY TEST
K920766 T4 EIA BEAD ASSAY
K920716 DIRECT PREGNANCY TEST
K902574 POTASSIUM REAGENT SET
K883387 ALANINE AMINO TRANSFERASE (COLORIMETRIC METHOD)
K883683 HEMOGLOBIN
K883386 CHLORIDE
K881172 BILIRUBIN (DIRECT)
K881173 ASPARTATE AMINOTRANSFERASE (COLORIMETRIC METHOD)
Search all 36 clearances from Tech-Co, Inc. →