Cleared Traditional

K830326 - NEGATIVE PRESSURE ARTERIAL BLOOD LINE

K830326 is an FDA 510(k) clearance for NEGATIVE PRESSURE ARTERIAL BLOOD LINE, manufactured by Erika, Inc.. The device is a Class 1 General & Plastic Surgery device with product code KDC cleared through the Traditional 510(k) pathway after a 27-day FDA review.

K830326 · Erika, Inc. · General & Plastic Surgery device
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Feb 1983
Decision
27d
Days
Class 1
Risk

K830326 is an FDA 510(k) clearance for the NEGATIVE PRESSURE ARTERIAL BLOOD LINE. Classified as Instrument, Surgical, Disposable (product code KDC), Class I - General Controls.

Submitted by Erika, Inc. (Mchenry, US). The FDA issued a Cleared decision on February 28, 1983 after a review of 27 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 Erika, Inc. devices

FDA 510(k) Submission Details - K830326

510(k) Number K830326 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 01, 1983
Decision Date February 28, 1983
Days to Decision 27 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
88d faster than avg
Panel avg: 115d · This submission: 27d
Pathway characteristics
Predicate-based equivalence.

KDC Device Classification - Class 1, General Controls

Product Code KDC Instrument, Surgical, Disposable
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.

Regulatory Peers - KDC Instrument, Surgical, Disposable

All 24
Devices cleared under the same product code (KDC) and FDA review panel - the closest regulatory comparables to K830326.
C-LOOPS
K830800 · Concept, Inc. · Oct 1983
DISPOSABLE SCALPELS
K831798 · I M, Inc. · Jul 1983
DEVO'N LOOPS
K830248 · Devon Industries, Inc. · Mar 1983
KAM SUCKER
K822065 · The Anspach Effort, Inc. · Aug 1982
KOLOR KODE TM
K821166 · Devon Industries, Inc. · May 1982
PEDIATRIC SUCKER
K820638 · 3M Health Care, Sarns · Apr 1982