Cleared Traditional

K883463 - HOSPITAL BED CLOTHING CRADLE

K883463 is the FDA 510(k) clearance for HOSPITAL BED CLOTHING CRADLE by Commercial Products & Engineering Co.. It is a Class 2 General Hospital device (product code FNL) cleared through the Traditional 510(k) pathway after a 35-day FDA review.

K883463 · Commercial Products & Engineering Co. · General Hospital
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Sep 1988
Decision
35d
Days
Class 2
Risk

K883463 is an FDA 510(k) clearance for the HOSPITAL BED CLOTHING CRADLE. Classified as Bed, Ac-powered Adjustable Hospital (product code FNL), Class II - Special Controls.

Submitted by Commercial Products & Engineering Co. (Grand Rapids, US). The FDA issued a Cleared decision on September 19, 1988 after a review of 35 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5100 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Commercial Products & Engineering Co. devices

Submission Details

510(k) Number K883463 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 15, 1988
Decision Date September 19, 1988
Days to Decision 35 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
94d faster than avg
Panel avg: 129d · This submission: 35d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code FNL Bed, Ac-powered Adjustable Hospital
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5100
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 - FNL Bed, Ac-powered Adjustable Hospital

All 16
Devices cleared under the same product code (FNL) and FDA review panel - the closest regulatory comparables to K883463.
THE ADVANCE SERIES FROM HILL-ROM
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