Cleared Traditional

K801942 - OHIO THORACIC COLLECTION UNIT

K801942 is the FDA 510(k) clearance for OHIO THORACIC COLLECTION UNIT by Ohio Medical Products. It is a Class 2 General Hospital device (product code GCX) cleared through the Traditional 510(k) pathway after a 34-day FDA review.

K801942 · Ohio Medical Products · General Hospital
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Sep 1980
Decision
34d
Days
Class 2
Risk

K801942 is an FDA 510(k) clearance for the OHIO THORACIC COLLECTION UNIT. Classified as Apparatus, Suction, Operating-room, Wall Vacuum Powered (product code GCX), Class II - Special Controls.

Submitted by Ohio Medical Products (Mchenry, US). The FDA issued a Cleared decision on September 16, 1980 after a review of 34 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6740 - 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 Ohio Medical Products devices

Submission Details

510(k) Number K801942 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 13, 1980
Decision Date September 16, 1980
Days to Decision 34 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
95d faster than avg
Panel avg: 129d · This submission: 34d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GCX Apparatus, Suction, Operating-room, Wall Vacuum Powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.6740
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 - GCX Apparatus, Suction, Operating-room, Wall Vacuum Powered

All 25
Devices cleared under the same product code (GCX) and FDA review panel - the closest regulatory comparables to K801942.
SURGICAL SUCTION INSTRUMENTS-DISPOS.
K812845 · Abco Dealers, Inc. · Nov 1981
ARGYLE YANKAUER SUCTION TUBE
K813066 · Sherwood Medical Co. · Nov 1981
ARGYLE COMPACT CHEST DRAINAGE SYS.
K802440 · Sherwood Medical Co. · Oct 1980
ARGYLE COMPACT CHEST DRAINAGE SYSTEM
K801979 · Sherwood Medical Co. · Sep 1980
TUBING, DYNACOR UNIVERSAL
K790055 · Medline Industries, Inc. · Feb 1979
SUCTION INSTRUMENT, MACBICK POOLE TIP
K760216 · C.R. Bard, Inc. · Aug 1976