Cleared Traditional

K932757 - SECURODRIP (TM) I.V. ARMBOARD

K932757 is an FDA 510(k) clearance for SECURODRIP (TM) I.V. ARMBOARD, manufactured by Op-Co Medical Products , Ltd.. The device is a Class 1 General Hospital device with product code KMK cleared through the Traditional 510(k) pathway after a 187-day FDA review.

K932757 · Op-Co Medical Products , Ltd. · General Hospital
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Dec 1993
Decision
187d
Days
Class 1
Risk

K932757 is an FDA 510(k) clearance for the SECURODRIP (TM) I.V. ARMBOARD. Classified as Device, Intravascular Catheter Securement (product code KMK), Class I - General Controls.

Submitted by Op-Co Medical Products , Ltd. (New York City, US). The FDA issued a Cleared decision on December 8, 1993 after a review of 187 days - an extended review cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5210 - the FDA general hospital 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Op-Co Medical Products , Ltd. devices

FDA 510(k) Submission Details - K932757

510(k) Number K932757 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 04, 1993
Decision Date December 08, 1993
Days to Decision 187 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
58d slower than avg
Panel avg: 129d · This submission: 187d
Pathway characteristics
Predicate-based equivalence.

KMK Device Classification - Class 1, General Controls

Product Code KMK Device, Intravascular Catheter Securement
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.5210
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 - KMK Device, Intravascular Catheter Securement

All 14
Devices cleared under the same product code (KMK) and FDA review panel - the closest regulatory comparables to K932757.
MULTI-PURPOSE MEDICAL TUBE HOLDER
K963365 · Byrd Medical Devices, Inc. · Oct 1996
CONMED VENI-GARD I.V. DRESSING
K935389 · Conmedcorp · Mar 1994
CENTERMARK SECURING WINGS
K940127 · Menlo Care, Inc. · Feb 1994
DUODERM TRANSPARENT HYDROCOLLOID DRESSING
K925992 · Convatec, A Division of E.R. Squibb & Sons · Oct 1993
IAB ANCHOR
K922103 · Datascope Corp. · Aug 1993
DESERET POSITIONAL SUTURE WING
K915495 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Apr 1992