Cleared Traditional

K913884 - FUJI II LC

K913884 is an FDA 510(k) clearance for FUJI II LC, manufactured by G-C Intl. Corp.. The device is a Class 2 Dental device with product code EMA cleared through the Traditional 510(k) pathway after a 62-day FDA review.

K913884 · G-C Intl. Corp. · Dental device
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Oct 1991
Decision
62d
Days
Class 2
Risk

K913884 is an FDA 510(k) clearance for the FUJI II LC. Classified as Cement, Dental (product code EMA), Class II - Special Controls.

Submitted by G-C Intl. Corp. (Scottsdale, US). The FDA issued a Cleared decision on October 30, 1991 after a review of 62 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3275 - the FDA dental device regulatory 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 G-C Intl. Corp. devices

FDA 510(k) Submission Details - K913884

510(k) Number K913884 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 29, 1991
Decision Date October 30, 1991
Days to Decision 62 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
65d faster than avg
Panel avg: 127d · This submission: 62d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EMA Device Classification - Class 2, Special Controls

Product Code EMA Cement, Dental
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3275
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 Dental devices follow this clearance model.

Regulatory Peers - EMA Cement, Dental

All 338
Devices cleared under the same product code (EMA) and FDA review panel - the closest regulatory comparables to K913884.
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K913572 · Specialites Septodont · Oct 1991