Cleared Traditional

K971063 - OPTIMA PLUS E DENTAL CHAIR

Also marketed or referenced as:
A DENTAL CHAIR EXCEL CHAIR

K971063 is an FDA 510(k) clearance for OPTIMA PLUS E DENTAL CHAIR, manufactured by King Dental Corp.. The device is a Class 1 Dental device with product code KLC cleared through the Traditional 510(k) pathway after a 71-day FDA review.

K971063 · King Dental Corp. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 1997
Decision
71d
Days
Class 1
Risk

K971063 is an FDA 510(k) clearance for the OPTIMA PLUS E DENTAL CHAIR. Classified as Chair, Dental, With Operative Unit (product code KLC), Class I - General Controls.

Submitted by King Dental Corp. (Miami, US). The FDA issued a Cleared decision on June 3, 1997 after a review of 71 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.6250 - 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 King Dental Corp. devices

FDA 510(k) Submission Details - K971063

510(k) Number K971063 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 24, 1997
Decision Date June 03, 1997
Days to Decision 71 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
56d faster than avg
Panel avg: 127d · This submission: 71d
Pathway characteristics
Predicate-based equivalence.

KLC Device Classification - Class 1, General Controls

Product Code KLC Chair, Dental, With Operative Unit
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 872.6250
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 - KLC Chair, Dental, With Operative Unit

All 27
Devices cleared under the same product code (KLC) and FDA review panel - the closest regulatory comparables to K971063.
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