Cleared Traditional

K911508 - MAGNA SURGEONS GOWNS

K911508 is an FDA 510(k) clearance for MAGNA SURGEONS GOWNS, manufactured by Dms Miami, Inc.. The device is a Class 2 General Hospital device with product code FYA cleared through the Traditional 510(k) pathway after a 75-day FDA review.

K911508 · Dms Miami, Inc. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 1991
Decision
75d
Days
Class 2
Risk

K911508 is an FDA 510(k) clearance for the MAGNA SURGEONS GOWNS. Classified as Gown, Surgical (product code FYA), Class II - Special Controls.

Submitted by Dms Miami, Inc. (Vega Baja, GW). The FDA issued a Cleared decision on June 17, 1991 after a review of 75 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 Dms Miami, Inc. devices

FDA 510(k) Submission Details - K911508

510(k) Number K911508 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 03, 1991
Decision Date June 17, 1991
Days to Decision 75 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
54d faster than avg
Panel avg: 129d · This submission: 75d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FYA Device Classification - Class 2, Special Controls

Product Code FYA Gown, 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 - FYA Gown, Surgical

All 237
Devices cleared under the same product code (FYA) and FDA review panel - the closest regulatory comparables to K911508.
BARRIER SURGICAL GOWN WITH SYMETRY FABRIC
K920996 · Johnson & Johnson Medical, Inc. · May 1992
STERILE CONVERTOR SAFECARE GOWN AND DRAPE
K920837 · Baxter Healthcare Corp · May 1992
COMPEL E
K914839 · Standard Textile Co., Inc. · Apr 1992
STERILE VIEW DISP. HOOD/GOWN UV, BARRIER HOOD, UV
K901536 · Depuy, Inc. · Nov 1990
CONVERTORS BREATHABLE GOWN MATERIAL PRODUCT LINE
K896935 · Baxter Healthcare Corp · Feb 1990
KIMBERLY-CLARK IMPERVIOUS OPEN BACK GOWN
K880382 · Kimberly-Clark Corp. · Jun 1988