Cleared Traditional

K101551 - PACEMAKER HIGH-SPEED HANDPIECE MODEL PM-MQ, PM-M

K101551 is an FDA 510(k) clearance for PACEMAKER HIGH-SPEED HANDPIECE MODEL PM-MQ, manufactured by Delma Medical Instrument (Guangzhou) Co., Ltd.. The device is a Class 1 Dental device with product code EFB cleared through the Traditional 510(k) pathway after a 97-day FDA review.

K101551 · Delma Medical Instrument (Guangzhou) Co., Ltd. · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 2010
Decision
97d
Days
Class 1
Risk

K101551 is an FDA 510(k) clearance for the PACEMAKER HIGH-SPEED HANDPIECE MODEL PM-MQ, PM-M. Classified as Handpiece, Air-powered, Dental (product code EFB), Class I - General Controls.

Submitted by Delma Medical Instrument (Guangzhou) Co., Ltd. (Dover, US). The FDA issued a Cleared decision on September 9, 2010 after a review of 97 days - within the typical 510(k) review window.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.4200 - 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 Delma Medical Instrument (Guangzhou) Co., Ltd. devices

FDA 510(k) Submission Details - K101551

510(k) Number K101551 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 04, 2010
Decision Date September 09, 2010
Days to Decision 97 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
30d faster than avg
Panel avg: 127d · This submission: 97d
Pathway characteristics
Predicate-based equivalence.

EFB Device Classification - Class 1, General Controls

Product Code EFB Handpiece, Air-powered, Dental
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 872.4200
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 - EFB Handpiece, Air-powered, Dental

All 107
Devices cleared under the same product code (EFB) and FDA review panel - the closest regulatory comparables to K101551.
PROPHY-MATE NEO
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EMS AIR-FLOW HANDY PERIO
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AIR TORX, MODEL TRA-200, TRA-200-CP3, TRA-200-CP4
K091065 · J. Morita USA, Inc. · Oct 2009