Cleared Traditional

K914749 - WAVICIDE(R) -01

K914749 is an FDA 510(k) clearance for WAVICIDE -01, manufactured by Wave Energy Systems, Inc.. The device is a Class 2 General Hospital device with product code MED cleared through the Traditional 510(k) pathway after a 1388-day FDA review.

K914749 · Wave Energy Systems, Inc. · General Hospital
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Aug 1995
Decision
1388d
Days
Class 2
Risk

K914749 is an FDA 510(k) clearance for the WAVICIDE(R) -01. Classified as Sterilant, Medical Devices (product code MED), Class II - Special Controls.

Submitted by Wave Energy Systems, Inc. (Cedar Grove, US). The FDA issued a Cleared decision on August 10, 1995 after a review of 1388 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6885 - 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind General Hospital submissions.

View all Wave Energy Systems, Inc. devices

FDA 510(k) Submission Details - K914749

510(k) Number K914749 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 22, 1991
Decision Date August 10, 1995
Days to Decision 1388 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
1259d slower than avg
Panel avg: 129d · This submission: 1388d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MED Device Classification - Class 2, Special Controls

Product Code MED Sterilant, Medical Devices
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.6885
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 - MED Sterilant, Medical Devices

All 53
Devices cleared under the same product code (MED) and FDA review panel - the closest regulatory comparables to K914749.
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K915170 · Pymah Corp. · Jul 1992