Cleared Traditional

K801589 - AUTO SUTURE DISP. 30, ETC. & SURG. STAP (FDA 510(k) Clearance)

Class I General & Plastic Surgery device.

K801589 · United States Surgical, A Division of Tyco Healthc · General & Plastic Surgery device
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Aug 1980
Decision
24d
Days
Class 1
Risk

K801589 is an FDA 510(k) clearance for the AUTO SUTURE DISP. 30, ETC. & SURG. STAP. Classified as Apparatus, Suturing, Stomach And Intestinal (product code FHM), Class I - General Controls.

Submitted by United States Surgical, A Division of Tyco Healthc (Mchenry, US). The FDA issued a Cleared decision on August 4, 1980 after a review of 24 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4800 - the FDA general and plastic surgery 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 United States Surgical, A Division of Tyco Healthc devices

Submission Details

510(k) Number K801589 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 11, 1980
Decision Date August 04, 1980
Days to Decision 24 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
90d faster than avg
Panel avg: 114d · This submission: 24d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code FHM Apparatus, Suturing, Stomach And Intestinal
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4800
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.