Cleared Traditional

K904045 - #504 MINI COMPRESSOR

K904045 is an FDA 510(k) clearance for #504 MINI COMPRESSOR, manufactured by Medical Industries America, Inc.. The device is a Class 2 Anesthesiology device with product code BTI cleared through the Traditional 510(k) pathway after a 161-day FDA review.

K904045 · Medical Industries America, Inc. · Anesthesiology device
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Feb 1991
Decision
161d
Days
Class 2
Risk

K904045 is an FDA 510(k) clearance for the #504 MINI COMPRESSOR. Classified as Compressor, Air, Portable (product code BTI), Class II - Special Controls.

Submitted by Medical Industries America, Inc. (Adel, US). The FDA issued a Cleared decision on February 12, 1991 after a review of 161 days - an extended review cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.6250 - the FDA anesthesiology and respiratory device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Anesthesiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Medical Industries America, Inc. devices

FDA 510(k) Submission Details - K904045

510(k) Number K904045 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 04, 1990
Decision Date February 12, 1991
Days to Decision 161 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
21d slower than avg
Panel avg: 140d · This submission: 161d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BTI Device Classification - Class 2, Special Controls

Product Code BTI Compressor, Air, Portable
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.6250
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Anesthesiology devices follow this clearance model.

Regulatory Peers - BTI Compressor, Air, Portable

All 26
Devices cleared under the same product code (BTI) and FDA review panel - the closest regulatory comparables to K904045.
SAM ST
K913097 · Ferguson Medical · Dec 1992
NEBULIZER SYSTEM
K922623 · Healthdyne, Inc. · Dec 1992
AIR STAR
K920954 · Infrasonics Corp. · Aug 1992
PM14 SOFT AIR COMPRESSOR
K902762 · Precision Medical, Inc. · Jul 1990
ECONO-MIST PORTABLE COMPRESSOR DRIVEN NEBULIZER
K873677 · Mountain Medical Equipment, Inc. · Oct 1987
SIEMENS DRY AIR COMPRESSOR
K871829 · Siemens Elema AB · Jun 1987