Cleared Traditional

K971727 - DCI WATER PURIFIER

K971727 is an FDA 510(k) clearance for DCI WATER PURIFIER, manufactured by Dental Components, Inc.. The device is a Class 1 Dental device with product code EIA cleared through the Traditional 510(k) pathway after a 126-day FDA review.

K971727 · Dental Components, Inc. · Dental device
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Sep 1997
Decision
126d
Days
Class 1
Risk

K971727 is an FDA 510(k) clearance for the DCI WATER PURIFIER. Classified as Unit, Operative Dental (product code EIA), Class I - General Controls.

Submitted by Dental Components, Inc. (Newberg, US). The FDA issued a Cleared decision on September 12, 1997 after a review of 126 days - within the typical 510(k) review window.

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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Dental review framework, consistent with the majority of Class II 510(k) submissions.

View all Dental Components, Inc. devices

FDA 510(k) Submission Details - K971727

510(k) Number K971727 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 09, 1997
Decision Date September 12, 1997
Days to Decision 126 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
1d faster than avg
Panel avg: 127d · This submission: 126d
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 109
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