510(k) K903638

GASTRO-INTESTINAL ACCU-CULSHURE TM by Medical Laboratory Automation Systems, Inc. — Product Code LIO

K903638 is an FDA 510(k) premarket notification submitted by Medical Laboratory Automation Systems, Inc. for the device "GASTRO-INTESTINAL ACCU-CULSHURE TM". The FDA issued a decision of Substantially Equivalent on January 18, 1991. The device falls under product code LIO (Device, Specimen Collection), a Class I device regulated under 21 CFR 866.2900. Medical Laboratory Automation Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 18, 1991
Date Received
August 13, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Specimen Collection
Device Class
Class I
Regulation Number
866.2900
Review Panel
MI
Submission Type