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

ARCHITECT T-UPTAKE CALIBRATORS (A-F) AND CONTROLS (LOW, HIGH)

K Number: K042307 · Decision Nov 3, 2004
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
244
Applicant Total
28
Review Days
70

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Basic Information

Device Name
ARCHITECT T-UPTAKE CALIBRATORS (A-F) AND CONTROLS (LOW, HIGH)
K Number
K042307
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
862.1150
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Seradyn, Inc.
Date Received
August 25, 2004
Decision Date
November 3, 2004
Product Code
JIT
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
JIT Calibrator, Secondary

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