Cleared Traditional

SUNPAK AQUA FLOSS 2000 CORDLESS PERSONAL ORAL JET (K900991) - FDA 510(k) Clearance

Class I Dental device.

K900991 · Tocad America, Inc. · Dental device
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May 1990
Decision
74d
Days
Class 1
Risk

K900991 is an FDA 510(k) clearance for the SUNPAK AQUA FLOSS 2000 CORDLESS PERSONAL ORAL JET. Classified as Unit, Oral Irrigation (product code EFS), Class I - General Controls.

Submitted by Tocad America, Inc. (Washington, US). The FDA issued a Cleared decision on May 15, 1990 after a review of 74 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.6510 - 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 Tocad America, Inc. devices

Submission Details

510(k) Number K900991 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 02, 1990
Decision Date May 15, 1990
Days to Decision 74 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
53d faster than avg
Panel avg: 127d · This submission: 74d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code EFS Unit, Oral Irrigation
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 872.6510
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.