Cleared Traditional

K812747 - ARGYLE SUCTION CATHETERS

K812747 is the FDA 510(k) clearance for ARGYLE SUCTION CATHETERS by Sherwood Medical Co.. It is a Class 1 Anesthesiology device (product code BSY) cleared through the Traditional 510(k) pathway after a 24-day FDA review.

K812747 · Sherwood Medical Co. · Anesthesiology device
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Oct 1981
Decision
24d
Days
Class 1
Risk

K812747 is an FDA 510(k) clearance for the ARGYLE SUCTION CATHETERS. Classified as Catheters, Suction, Tracheobronchial (product code BSY), Class I - General Controls.

Submitted by Sherwood Medical Co. (Mchenry, US). The FDA issued a Cleared decision on October 23, 1981 after a review of 24 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.6810 - 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 Sherwood Medical Co. devices

Submission Details

510(k) Number K812747 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 29, 1981
Decision Date October 23, 1981
Days to Decision 24 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
116d faster than avg
Panel avg: 140d · This submission: 24d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code BSY Catheters, Suction, Tracheobronchial
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 868.6810
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.

Regulatory Peers - BSY Catheters, Suction, Tracheobronchial

All 36
Devices cleared under the same product code (BSY) and FDA review panel - the closest regulatory comparables to K812747.
ACKRAD BRONCHITRAC
K822398 · Ackrad Laboratories · Oct 1982
SUCTION CATHETERS & KITS
K820369 · American Pharmaseal Div. Ahsc · Apr 1982
RADIATION STERILIZED SUCTION CATHETERS
K820109 · Travenol Laboratories, S.A. · Jan 1982
HYDROPHILIC COATED CATHETER
K810023 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Feb 1981
CATHETER SUCTION TRACHEOBRONCHIAL
K801814 · Concord Laboratories, Inc. · Aug 1980
ARGYLE SAF-T-MARK SUCTION CATHETER
K801551 · Sherwood Medical Co. · Jul 1980