Cleared Traditional

K030239 - MEGATECH SCIENTIFIC FACE MASK

K030239 is an FDA 510(k) clearance for MEGATECH SCIENTIFIC FACE MASK, manufactured by Megatech Scientific Pte, Ltd.. The device is a Class 2 General Hospital device with product code FXX cleared through the Traditional 510(k) pathway after a 182-day FDA review.

K030239 · Megatech Scientific Pte, Ltd. · General Hospital
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Jul 2003
Decision
182d
Days
Class 2
Risk

K030239 is an FDA 510(k) clearance for the MEGATECH SCIENTIFIC FACE MASK. Classified as Mask, Surgical (product code FXX), Class II - Special Controls.

Submitted by Megatech Scientific Pte, Ltd. (Skytech #09-03, SG). The FDA issued a Cleared decision on July 24, 2003 after a review of 182 days - an extended review 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Megatech Scientific Pte, Ltd. devices

FDA 510(k) Submission Details - K030239

510(k) Number K030239 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 23, 2003
Decision Date July 24, 2003
Days to Decision 182 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
53d slower than avg
Panel avg: 129d · This submission: 182d
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 492
Devices cleared under the same product code (FXX) and FDA review panel - the closest regulatory comparables to K030239.
SURGICAL FACE MASK
K110027 · Angeline Group , Ltd. · Aug 2011
KIMBERLY-CLARK LOW BARRIER, ASTM 2100 FACE MASKS
K110455 · Kimberly-Clark Corp. · Apr 2011
CROSSTEX SURGICAL EARLOOP MASK- WHITE, CROSSTEX SURGICAL EARLOOP NO FOG MASK-WHITE, NO FOG MASK WITH SPLASH VISOR-WHITE
K103303 · Crosstex International, Inc. · Dec 2010
HENRY SCHEIN SURGICAL MASK
K992604 · Mitsui Textile Corp. · Jan 2000
MEDLINE PROHIBIT SERIES SURGICAL MASK WITH FLUID SHIELD
K991559 · Medline Industries, Inc. · Aug 1999
EARLOOP FACE MASK
K990719 · Shuenn Bao Shing Corp. · Jul 1999