510(k) K902184

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

K902184 is an FDA 510(k) premarket notification submitted by Medical Industries America, Inc. for the device "MAXI ASPIRATOR". The FDA issued a decision of Substantially Equivalent on February 12, 1991. 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
February 12, 1991
Date Received
May 14, 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