Cleared Traditional

K843906 - SNYDER HEMOVAC WOUND DRAINAGE DEVICES

K843906 is the FDA 510(k) clearance for SNYDER HEMOVAC WOUND DRAINAGE DEVICES by Snyder Laboratories, Inc.. It is a Class 1 General & Plastic Surgery device (product code GBS) cleared through the Traditional 510(k) pathway after a 33-day FDA review.

K843906 · Snyder Laboratories, Inc. · General & Plastic Surgery device
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Nov 1984
Decision
33d
Days
Class 1
Risk

K843906 is an FDA 510(k) clearance for the SNYDER HEMOVAC WOUND DRAINAGE DEVICES. Classified as Catheter, Ventricular, General & Plastic Surgery (product code GBS), Class I - General Controls.

Submitted by Snyder Laboratories, Inc. (New Philadelphia, US). The FDA issued a Cleared decision on November 5, 1984 after a review of 33 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4200 - 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 Snyder Laboratories, Inc. devices

Submission Details

510(k) Number K843906 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 03, 1984
Decision Date November 05, 1984
Days to Decision 33 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
82d faster than avg
Panel avg: 115d · This submission: 33d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code GBS Catheter, Ventricular, General & Plastic Surgery
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 878.4200
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 - GBS Catheter, Ventricular, General & Plastic Surgery

All 7
Devices cleared under the same product code (GBS) and FDA review panel - the closest regulatory comparables to K843906.
ATRIUMS PDR THORACIC CATHETER
K912645 · Atrium Medical Corp. · Sep 1991
CLOSED CHEST DRAINAGE SET W/SUTURES
K873377 · Gish Biomedical, Inc. · Oct 1987
OSTEOTOMY DRAINAGE TUBE
K862584 · Treace Medical, Inc. · Aug 1986
ARGYLE MEDIASTINAL DRAIN
K822318 · Sherwood Medical Co. · Aug 1982
SIL-V-UR CHEST CATHETER
K813463 · C.R. Bard, Inc. · Feb 1982
DAVOL SILICONE SHEATH SUMP DRAIN
K810158 · C.R. Bard, Inc. · Feb 1981