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

MODIFICATION TO: I-STAT PORTABLE CLINICAL ANALYZER

K Number: K012478 · Decision Aug 20, 2001
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
187
Applicant Total
14
Review Days
18

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Basic Information

Device Name
MODIFICATION TO: I-STAT PORTABLE CLINICAL ANALYZER
K Number
K012478
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
862.1120
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
I-Stat Corp.
Date Received
August 2, 2001
Decision Date
August 20, 2001
Product Code
CHL
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
CHL Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph

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Other Clearances by I-Stat Corp.

K Number Device Name
K011478 I-STAT SYSTEM
K001387 I-STAT PORTABLE CLINICAL ANALYZER, MODEL 300
K001154 I-STAT MODEL 200 PORTABLE CLINICAL ANALYZER
K992571 I-STAT SYSTEM
K982071 I-STAT LACTATE TEST
K973292 I-STAT SYSTEM
K940918 I-STAT 200 PORTABLE CLINICAL ANALYZER
K936081 I-STAT TESTS FOR ACID-BASE PARAMETERS
K934642 I-STAT IONIZED CALCIUM TEST
K934641 I-STAT CONTROL LEVELS 1,2,3
Search all 14 clearances from I-Stat Corp. →