Cleared Traditional

K910410 - SURGICAL GOWNS, EXTRA-LARGE SIZE

K910410 is an FDA 510(k) clearance for SURGICAL GOWNS, manufactured by Dawn of Hope Development Center. The device is a Class 2 General Hospital device with product code FYC cleared through the Traditional 510(k) pathway after a 86-day FDA review.

K910410 · Dawn of Hope Development Center · General Hospital
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Apr 1991
Decision
86d
Days
Class 2
Risk

K910410 is an FDA 510(k) clearance for the SURGICAL GOWNS, EXTRA-LARGE SIZE. Classified as Gown, Isolation, Surgical (product code FYC), Class II - Special Controls.

Submitted by Dawn of Hope Development Center (Johnson City, US). The FDA issued a Cleared decision on April 25, 1991 after a review of 86 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 Dawn of Hope Development Center devices

FDA 510(k) Submission Details - K910410

510(k) Number K910410 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 29, 1991
Decision Date April 25, 1991
Days to Decision 86 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
43d faster than avg
Panel avg: 129d · This submission: 86d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FYC Device Classification - Class 2, Special Controls

Product Code FYC Gown, Isolation, 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 - FYC Gown, Isolation, Surgical

All 48
Devices cleared under the same product code (FYC) and FDA review panel - the closest regulatory comparables to K910410.
COVER GOWN
K952116 · American Threshold Industries, Inc. · Sep 1995
BUSE STAFF PROTECTION GOWNS AND KITS
K941845 · Busse Hospital Disposables, Inc. · May 1995
OREX ISOLATION GOWN
K945223 · Thantex Specialties, Inc. · Apr 1995
ISOLATION GOWN
K874888 · Sage Products, Inc. · Dec 1987
MAXIMUM CONTROL GOWN
K874318 · Ulti-Med Intl., Inc. · Dec 1987
DISPOSABLE ISOLATION GOWN
K851823 · American Threshold Industries, Inc. · May 1985