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

BIOTRACK THEOPHYLLINE QUALITY CONTROLS

K Number: K903924 · Decision Sep 17, 1990
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
3
Applicant Total
16
Review Days
24

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Basic Information

Device Name
BIOTRACK THEOPHYLLINE QUALITY CONTROLS
K Number
K903924
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.3280
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
Biotrack, Inc.
Date Received
August 24, 1990
Decision Date
September 17, 1990
Product Code
LAW
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LAW Theophylline Control Materials

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Other Clearances by Biotrack, Inc.

K Number Device Name
K934061 BIOTRACK VALPROIC ACID TEST CARTRIDGE
K934062 BIOTRACK THERAPEUTIC DRUG-MONITORING QUAL CONTROLS
K920525 BIOTRACK THERAPEUTIC DRUG MONITORING QUAL. CONTROL
K915755 BIOTRACK PHENYTOIN TEST CARTRIDGE
K915756 BIOTRACK CARBAMAZEPINE TEST CARTRIDGE
K900373 BIOTRACK THEOPHYLLINE TEST CARTRIDGE
K900372 BIOTRACK IMMUNOCHEMISTRY MONITOR
K895101 BIOTRACK HEMOGLOBIN TEST CARTRIDGE
K895102 BIOTRACK PDS MONITOR
K895128 BIOTRACK ALT TEST CARTRIDGE
Search all 16 clearances from Biotrack, Inc. →