Cleared Traditional

K970002 - STERILE WATER PUMP

K970002 is an FDA 510(k) clearance for STERILE WATER PUMP, manufactured by Micro Motors, Inc.. The device is a Class 1 Dental device with product code EIA cleared through the Traditional 510(k) pathway after a 62-day FDA review.

K970002 · Micro Motors, Inc. · Dental device
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Mar 1997
Decision
62d
Days
Class 1
Risk

K970002 is an FDA 510(k) clearance for the STERILE WATER PUMP. Classified as Unit, Operative Dental (product code EIA), Class I - General Controls.

Submitted by Micro Motors, Inc. (Santa Ana, US). The FDA issued a Cleared decision on March 5, 1997 after a review of 62 days - a notably fast clearance cycle.

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: 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 Micro Motors, Inc. devices

FDA 510(k) Submission Details - K970002

510(k) Number K970002 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 02, 1997
Decision Date March 05, 1997
Days to Decision 62 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
65d faster than avg
Panel avg: 127d · This submission: 62d
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
Devices cleared under the same product code (EIA) and FDA review panel - the closest regulatory comparables to K970002.
ATRION MEDICAL AUTOGENOUS TISSUE COLLECTOR
K971100 · Atrion Medical Products, Inc. · May 1997
ODYSSEY I DENTAL WATER UNIT
K964796 · Germiphene Corp. · May 1997
EASY CAM
K970626 · I.C.S. · Apr 1997
DELIVERY SYSTEM(SDS 1400 XL)/DELIVERY SYSTEM CUSPIDOR(SDS1450,SDS1650 XL)
K964619 · Sds Dental, Inc. · Jan 1997
PROSTYLE COMPACT
K961420 · Planmeca Oy · Sep 1996
A-DEC SELF-CONTAINED WATER SYSTEM
K962665 · A-Dec, Inc. · Aug 1996