510(k) K900686

MAXI COMPRESSORS by Medical Industries America, Inc. — Product Code BTI

K900686 is an FDA 510(k) premarket notification submitted by Medical Industries America, Inc. for the device "MAXI COMPRESSORS". The FDA issued a decision of Substantially Equivalent on April 26, 1990. The device falls under product code BTI (Compressor, Air, Portable), a Class II device regulated under 21 CFR 868.6250. Medical Industries America, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 26, 1990
Date Received
February 13, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Compressor, Air, Portable
Device Class
Class II
Regulation Number
868.6250
Review Panel
AN
Submission Type