Cleared Traditional

K970440 - EKONIC DENTAL/MEDICAL MASK (MD 610)

K970440 is an FDA 510(k) clearance for EKONIC DENTAL/MEDICAL MASK (MD 610), manufactured by Ekonic Company, Ltd.. The device is a Class 2 General Hospital device with product code FXX cleared through the Traditional 510(k) pathway after a 50-day FDA review.

K970440 · Ekonic Company, Ltd. · General Hospital
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Mar 1997
Decision
50d
Days
Class 2
Risk

K970440 is an FDA 510(k) clearance for the EKONIC DENTAL/MEDICAL MASK (MD 610). Classified as Mask, Surgical (product code FXX), Class II - Special Controls.

Submitted by Ekonic Company, Ltd. (Carver, US). The FDA issued a Cleared decision on March 27, 1997 after a review of 50 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 878.4040 - the FDA general hospital device 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 Ekonic Company, Ltd. devices

FDA 510(k) Submission Details - K970440

510(k) Number K970440 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 05, 1997
Decision Date March 27, 1997
Days to Decision 50 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
79d faster than avg
Panel avg: 129d · This submission: 50d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FXX Device Classification - Class 2, Special Controls

Product Code FXX Mask, Surgical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4040
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General Hospital devices follow this clearance model.

Regulatory Peers - FXX Mask, Surgical

All 464
Devices cleared under the same product code (FXX) and FDA review panel - the closest regulatory comparables to K970440.
FLOOR MASK-EAR LOOP(BMR-15011)/FLOOR MASK-TIE(BMR-1503)
K971744 · Berkley Medical Resources, Inc. · Jul 1997
DEFEND FLUID RESISTANT PLEATED MASK
K971130 · Carl Parker Associates, Inc. · Jun 1997
DEPUY OPTI-CON AND E-Z SHIELD SYSTEMS
K964114 · Depuy, Inc. · May 1997
MEDLINE ADMISSION KITS
K965107 · Medline Industries, Inc. · Mar 1997
3M 1830 FLUID BLOCK ANTI-FOG TIE-ON SURGICAL MASK AND 3M 1830FS FLUID BLOCK ANTI-FOG TIE-ON SURGICAL MASK WITH FACE SHIE
K965043 · Minnesota Mining and Mfg. Co. · Mar 1997
PROCEDURE SPECIFIC KITS
K964168 · Sage Products, Inc. · Mar 1997