Cleared Traditional

K930144 - THE SCITECH ONE-DAY FILTER

K930144 is an FDA 510(k) clearance for THE SCITECH ONE-DAY FILTER, manufactured by Scitech Solutions, Inc.. The device is a Class 1 Dental device with product code EIA cleared through the Traditional 510(k) pathway after a 406-day FDA review.

K930144 · Scitech Solutions, Inc. · Dental device
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Feb 1994
Decision
406d
Days
Class 1
Risk

K930144 is an FDA 510(k) clearance for the THE SCITECH ONE-DAY FILTER. Classified as Unit, Operative Dental (product code EIA), Class I - General Controls.

Submitted by Scitech Solutions, Inc. (Seattle, US). The FDA issued a Cleared decision on February 22, 1994 after a review of 406 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.6640 - 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Dental submissions.

View all Scitech Solutions, Inc. devices

FDA 510(k) Submission Details - K930144

510(k) Number K930144 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 12, 1993
Decision Date February 22, 1994
Days to Decision 406 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
279d slower than avg
Panel avg: 127d · This submission: 406d
Pathway characteristics
Predicate-based equivalence.

EIA Device Classification - Class 1, General Controls

Product Code EIA Unit, Operative Dental
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 872.6640
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 - EIA Unit, Operative Dental

All 124
Devices cleared under the same product code (EIA) and FDA review panel - the closest regulatory comparables to K930144.
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