Cleared Traditional

K853345 - 31ST. CENTRUY MEDICAL CORP TIME BUYER 4...

K853345 is the FDA 510(k) clearance for 31ST. CENTRUY MEDICAL CORP TIME BUYER 4... by 31st. Centruy Medical Corp.. It is a Class 2 Anesthesiology device (product code BWC) cleared through the Traditional 510(k) pathway after a 50-day FDA review.

K853345 · 31st. Centruy Medical Corp. · Anesthesiology device
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Oct 1985
Decision
50d
Days
Class 2
Risk

K853345 is an FDA 510(k) clearance for the 31ST. CENTRUY MEDICAL CORP TIME BUYER 428905 US PE. Classified as Needle, Emergency Airway (product code BWC), Class II - Special Controls.

Submitted by 31st. Centruy Medical Corp. (Pittsburgh, US). The FDA issued a Cleared decision on October 1, 1985 after a review of 50 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5090 - 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: 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 31st. Centruy Medical Corp. devices

Submission Details

510(k) Number K853345 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 12, 1985
Decision Date October 01, 1985
Days to Decision 50 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
90d faster than avg
Panel avg: 140d · This submission: 50d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code BWC Needle, Emergency Airway
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5090
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.