Cleared Traditional

K801470 - MICRO CLIP STERILIZING CASE #65199

K801470 is an FDA 510(k) clearance for MICRO CLIP STERILIZING CASE #65199, manufactured by Edward Weck, Inc.. The device is a Class 1 General & Plastic Surgery device with product code FSM cleared through the Traditional 510(k) pathway after a 20-day FDA review.

K801470 · Edward Weck, Inc. · General & Plastic Surgery device
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Jul 1980
Decision
20d
Days
Class 1
Risk

K801470 is an FDA 510(k) clearance for the MICRO CLIP STERILIZING CASE #65199. Classified as Tray, Surgical, Instrument (product code FSM), Class I - General Controls.

Submitted by Edward Weck, Inc. (Mchenry, US). The FDA issued a Cleared decision on July 14, 1980 after a review of 20 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 Edward Weck, Inc. devices

FDA 510(k) Submission Details - K801470

510(k) Number K801470 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 24, 1980
Decision Date July 14, 1980
Days to Decision 20 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
95d faster than avg
Panel avg: 115d · This submission: 20d
Pathway characteristics
Predicate-based equivalence.

FSM Device Classification - Class 1, General Controls

Product Code FSM Tray, Surgical, Instrument
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 - FSM Tray, Surgical, Instrument

All 21
Devices cleared under the same product code (FSM) and FDA review panel - the closest regulatory comparables to K801470.
A.M.P.C.O. SKIN SCRUB TRAY
K802570 · Associated Medical Products Co. · Nov 1980
CUSTOM LYMPHANGIOGRAM ACCES. PACK-STERI
K801964 · American Pharmaseal Div. Ahsc · Oct 1980
CUSTOM UNIVERSAL CUTDOWN PREP TRAY
K801965 · American Pharmaseal Div. Ahsc · Oct 1980
MICRESURGICAL TRAY, SM.,MED., & LG.
K800367 · Edward Weck, Inc. · Mar 1980
WECK RACK (STERILIZING ACCESSORY TRAY)
K791743 · Edward Weck, Inc. · Sep 1979
ARMOR-KOT SURGICAL INSTRUMENTS
K771680 · Storz Instrument Co. · Nov 1977