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

CLINICAL CHLORIDE ANALYZER, CHLORIDE TEST SYSTEM, SWEAT CHLORIDE ANALYZER, CHLORIDOMETER, CHLORIDE COULOMETRIC

K Number: K121823 · Decision Mar 27, 2013
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
18
Applicant Total
13
Review Days
279

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Basic Information

Device Name
CLINICAL CHLORIDE ANALYZER, CHLORIDE TEST SYSTEM, SWEAT CHLORIDE ANALYZER, CHLORIDOMETER, CHLORIDE COULOMETRIC
K Number
K121823
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1170
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Wescor, Inc.
Date Received
June 21, 2012
Decision Date
March 27, 2013
Product Code
JFS
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
JFS Coulometric, Chloride

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Other Clearances by Wescor, Inc.

K Number Device Name
K010031 NANODUCT NEONATAL SWEAT ANALYSIS SYSTEM
K863395 WESCOR SWEAT.CHEK SWEAT CONDUCTIVITY ANALYZER
K881592 WESCOR MODEL 7300 AEROSPRAY GRAM STAINER
K881512 WESCOR GRAM STAIN PACK FOR MODEL 7300 AEROSPRAY
K880544 WESCOR STAIN CONCENTRATE FOR MODEL 7100 AEROSPRAY
K853973 WESCOR MODEL 3700 WEBSTER SWEAT INDUCER
K834214 WESCOR 5500 VAPOR PRESSURE OSMOMETER
K834208 COLLOID OSMOMETER 4400
K840472 SYS MACRODUCT SWEAT COLLECTION SYS 3600
K833295 WESCOR 7100 AEROSPRAY SLIDE STAINER
Search all 13 clearances from Wescor, Inc. →