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

VIRAL ACCU-CULSHURE TM

K Number: K903406 · Decision Oct 16, 1990
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
62
Applicant Total
17
Review Days
77

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Basic Information

Device Name
VIRAL ACCU-CULSHURE TM
K Number
K903406
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2900
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Medical Laboratory Automation Systems, Inc.
Date Received
July 31, 1990
Decision Date
October 16, 1990
Product Code
LIO
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
LIO Device, Specimen Collection

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Other Clearances by Medical Laboratory Automation Systems, Inc.

K Number Device Name
K962664 ELECTRA 1800C AUTOMATIC COAGULATION ANALYZER
K944227 ELECTRA 1400C AUTOMATIC COAGULATION ANALYZER
K931206 ELECTRA 1600C AUTOMATIC COAGULATION TIMER
K923220 THROMBIN CLOT TIME TEST PROCEDURE
K903638 GASTRO-INTESTINAL ACCU-CULSHURE TM
K903405 CHLAMYDIA ACCU-CULSHURE TM
K901645 ANAEROBIC ACCU-CULSHURE(TM)
K894052 ELECTRA 1000C AUTOMATIC COAGULATION TIMER
K884863 ELECTRA 900C AUTOMATIC COAGULATION TIMER
K871687 TYTEM(R) REAGENT DISPENSER
Search all 17 clearances from Medical Laboratory Automation Systems, Inc. →