Cleared Traditional

K924324 - K-1 INFANT TRANSPORT SYSTEM W/ INTEGRAL AIR COMPRE

K924324 is an FDA 510(k) clearance for K-1 INFANT TRANSPORT SYSTEM W/ INTEGRAL..., manufactured by K-1 Medical Products, Inc.. The device is a Class 2 General Hospital device with product code FMZ cleared through the Traditional 510(k) pathway after a 442-day FDA review.

K924324 · K-1 Medical Products, Inc. · General Hospital
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Nov 1993
Decision
442d
Days
Class 2
Risk

K924324 is an FDA 510(k) clearance for the K-1 INFANT TRANSPORT SYSTEM W/ INTEGRAL AIR COMPRE. Classified as Incubator, Neonatal (product code FMZ), Class II - Special Controls.

Submitted by K-1 Medical Products, Inc. (Sant Ee, US). The FDA issued a Cleared decision on November 12, 1993 after a review of 442 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5400 - the FDA general hospital 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind General Hospital submissions.

View all K-1 Medical Products, Inc. devices

FDA 510(k) Submission Details - K924324

510(k) Number K924324 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 27, 1992
Decision Date November 12, 1993
Days to Decision 442 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
313d slower than avg
Panel avg: 129d · This submission: 442d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FMZ Device Classification - Class 2, Special Controls

Product Code FMZ Incubator, Neonatal
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5400
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 General Hospital devices follow this clearance model.

Regulatory Peers - FMZ Incubator, Neonatal

All 62
Devices cleared under the same product code (FMZ) and FDA review panel - the closest regulatory comparables to K924324.
ISOLETTE INFANT INCUBATOR
K960980 · Air-Shields, Inc. · Jul 1996
OHIO CARE PLUS INCUBATOR
K943360 · Ohmeda Medical · Sep 1994
C450/C400 INFANT INCUBATORS
K940975 · Air-Shields, Inc. · Jun 1994
ISOLETTE INCUBATOR HUMIDITY METER
K924170 · Air-Shields, Inc. · Feb 1993
TYPE INTERFACE 9271/1 INCUBATOR/WARMER
K912000 · S & W Medico Teknik · Sep 1992
MODELS C500/C550 ISOLETE(R) INFANT INCUBATOR
K914864 · Air-Shields, Inc. · Mar 1992