Cleared Special

K110884 - EASYFIT SILKGEL NASAL MASK

K110884 is an FDA 510(k) clearance for EASYFIT SILKGEL NASAL MASK, manufactured by Weinmann Gerate Fur Medizin GmbH + Co. KG. The device is a Class 2 Anesthesiology device with product code BZD cleared through the Special 510(k) pathway after a 104-day FDA review.

K110884 · Weinmann Gerate Fur Medizin GmbH + Co. KG · Anesthesiology device
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Jul 2011
Decision
104d
Days
Class 2
Risk

K110884 is an FDA 510(k) clearance for the EASYFIT SILKGEL NASAL MASK. Classified as Ventilator, Non-continuous (respirator) (product code BZD), Class II - Special Controls.

Submitted by Weinmann Gerate Fur Medizin GmbH + Co. KG (Hamburg, DE). The FDA issued a Cleared decision on July 12, 2011 after a review of 104 days - within the typical 510(k) review window.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5905 - the FDA anesthesiology and respiratory device framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Standard predicate reliance. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Weinmann Gerate Fur Medizin GmbH + Co. KG devices

FDA 510(k) Submission Details - K110884

510(k) Number K110884 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 30, 2011
Decision Date July 12, 2011
Days to Decision 104 days
Submission Type Special
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
36d faster than avg
Panel avg: 140d · This submission: 104d
Pathway characteristics
Modification to existing cleared device.

BZD Device Classification - Class 2, Special Controls

Product Code BZD Ventilator, Non-continuous (respirator)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.5905
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 Anesthesiology devices follow this clearance model.

Regulatory Peers - BZD Ventilator, Non-continuous (respirator)

All 307
Devices cleared under the same product code (BZD) and FDA review panel - the closest regulatory comparables to K110884.
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