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

CHEMWELL, ALSO KNOWN AS PROJECT 2900

K Number: K013420 · Decision Jul 19, 2002
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
241
Applicant Total
18
Review Days
277

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Basic Information

Device Name
CHEMWELL, ALSO KNOWN AS PROJECT 2900
K Number
K013420
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
862.1690
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Awareness Technology, Inc.
Date Received
October 15, 2001
Decision Date
July 19, 2002
Product Code
JLW
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
JLW Radioimmunoassay, Thyroid-Stimulating Hormone

Similar 510(k) Clearances

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Other Clearances by Awareness Technology, Inc.

K Number Device Name
K171476 SelectaLyte Electrolyte Analyzer (Na+, K+, Cl-)
K010877 CHEMWELL, MODEL 2900
K974762 STAT TRACKS
K943729 DYE CHECK STRIPS 545-630
K941394 STAT FAX 2600
K923598 REDI-CHECK PHOTMETER Q.A.
K900224 STAT FAX(TM)-2100
K892656 DRI-DYE CHECK STRIPS (TM)-405
K882938 STAT FAX(TM)
K873451 PROJECT 300 MICROASSAY BP-12, EIA MINILAB
Search all 18 clearances from Awareness Technology, Inc. →