Cleared Traditional

K882240 - STORZ UNIV IRRIGAT/ASPIRA & PHACOEMULSI...

K882240 is the FDA 510(k) clearance for STORZ UNIV IRRIGAT/ASPIRA & PHACOEMULSI... by Storz Instrument Co.. It is a Class 1 General & Plastic Surgery device (product code GDM) cleared through the Traditional 510(k) pathway after a 63-day FDA review.

K882240 · Storz Instrument Co. · General & Plastic Surgery device
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Jul 1988
Decision
63d
Days
Class 1
Risk

K882240 is an FDA 510(k) clearance for the STORZ UNIV IRRIGAT/ASPIRA & PHACOEMULSIFCATION PAC. Classified as Needle, Aspiration And Injection, Reusable (product code GDM), Class I - General Controls.

Submitted by Storz Instrument Co. (St. Louis, US). The FDA issued a Cleared decision on July 29, 1988 after a review of 63 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 Storz Instrument Co. devices

Submission Details

510(k) Number K882240 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 27, 1988
Decision Date July 29, 1988
Days to Decision 63 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
52d faster than avg
Panel avg: 115d · This submission: 63d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code GDM Needle, Aspiration And Injection, Reusable
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 - GDM Needle, Aspiration And Injection, Reusable

All 15
Devices cleared under the same product code (GDM) and FDA review panel - the closest regulatory comparables to K882240.
MANAN BONE BIOPSY NEEDLE
K902177 · Manan Medical Products, Inc. · Sep 1990
PLEURA BIOPSY DEVICE
K901995 · Mill-Rose Laboratory · Jul 1990
CORE BIOPSY NEEDLE, CATALOG CODE #54006
K891537 · Dlp, Inc. · Apr 1989
E-Z-EM(R) LUFKIN BIOPSY NEEDLES
K882601 · E-Z-Em, Inc. · Jul 1988
WHOLEY (TM) BIOPSY DEVICE
K874928 · Medrad, Inc. · Dec 1987
CIVCO/KEMPF ASPIRATION/BIOPSY/DIALYSIS NEEDLE
K862481 · CIVCO Medical Instruments Co., Inc. · Jul 1986