Cleared Traditional

K946019 - SURGICLA INSTRUMENT KIT

K946019 is an FDA 510(k) clearance for SURGICLA INSTRUMENT KIT, manufactured by Medical Action Industries, Inc.. The device is a Class 2 General Hospital device with product code FRG cleared through the Traditional 510(k) pathway after a 98-day FDA review.

K946019 · Medical Action Industries, Inc. · General Hospital
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Mar 1995
Decision
98d
Days
Class 2
Risk

K946019 is an FDA 510(k) clearance for the SURGICLA INSTRUMENT KIT. Classified as Wrap, Sterilization (product code FRG), Class II - Special Controls.

Submitted by Medical Action Industries, Inc. (Asheville, US). The FDA issued a Cleared decision on March 20, 1995 after a review of 98 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6850 - 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 Medical Action Industries, Inc. devices

FDA 510(k) Submission Details - K946019

510(k) Number K946019 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 12, 1994
Decision Date March 20, 1995
Days to Decision 98 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
31d faster than avg
Panel avg: 129d · This submission: 98d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FRG Device Classification - Class 2, Special Controls

Product Code FRG Wrap, Sterilization
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.6850
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General Hospital devices follow this clearance model.

Regulatory Peers - FRG Wrap, Sterilization

All 233
Devices cleared under the same product code (FRG) and FDA review panel - the closest regulatory comparables to K946019.
G.E. STERILE PUNCTURE TRAY
K960202 · GE Medical Systems · Feb 1996
LACERATION TRAY
K955658 · Transidyne General Corp. · Jan 1996
STERIMED STERIZATION WRAPPER (NON-STERILE)
K953678 · Customed, Inc. · Oct 1995
SAFEDWEEL DRESSING CHANGE TRAY
K950438 · Becton Dickinson Vascular Access, Inc. · Mar 1995
MAMMOCORE BIOPSY TRAY
K943653 · Manan Medical Products, Inc. · Jan 1995
BIOPSY TRAY
K941645 · Cush Medical Products · Jul 1994