Cleared Traditional

K915207 - DISPOSABLE RADIOLUCENT RUBBER DAM CLAMP

K915207 is an FDA 510(k) clearance for DISPOSABLE RADIOLUCENT RUBBER DAM CLAMP, manufactured by Bay Technical Products, Inc.. The device is a Class 1 Dental device with product code EEF cleared through the Traditional 510(k) pathway after a 88-day FDA review.

K915207 · Bay Technical Products, Inc. · Dental device
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Feb 1992
Decision
88d
Days
Class 1
Risk

K915207 is an FDA 510(k) clearance for the DISPOSABLE RADIOLUCENT RUBBER DAM CLAMP. Classified as Clamp, Rubber Dam (product code EEF), Class I - General Controls.

Submitted by Bay Technical Products, Inc. (Fremont, US). The FDA issued a Cleared decision on February 14, 1992 after a review of 88 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.6300 - 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 Bay Technical Products, Inc. devices

FDA 510(k) Submission Details - K915207

510(k) Number K915207 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 18, 1991
Decision Date February 14, 1992
Days to Decision 88 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
39d faster than avg
Panel avg: 127d · This submission: 88d
Pathway characteristics
Predicate-based equivalence.

EEF Device Classification - Class 1, General Controls

Product Code EEF Clamp, Rubber Dam
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 872.6300
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.