Cleared Traditional

K981073 - MEDCOM GOWN PACK, MEDCOM DRAPE PACK & MEDCOM TOWEL PACK

K981073 is an FDA 510(k) clearance for MEDCOM GOWN PACK, manufactured by Medcom Laundry Service, Inc.. The device is a Class 2 General Hospital device with product code FYA cleared through the Traditional 510(k) pathway after a 52-day FDA review.

K981073 · Medcom Laundry Service, Inc. · General Hospital
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May 1998
Decision
52d
Days
Class 2
Risk

K981073 is an FDA 510(k) clearance for the MEDCOM GOWN PACK, MEDCOM DRAPE PACK & MEDCOM TOWEL PACK. Classified as Gown, Surgical (product code FYA), Class II - Special Controls.

Submitted by Medcom Laundry Service, Inc. (Fort Collins, US). The FDA issued a Cleared decision on May 15, 1998 after a review of 52 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 Medcom Laundry Service, Inc. devices

FDA 510(k) Submission Details - K981073

510(k) Number K981073 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 24, 1998
Decision Date May 15, 1998
Days to Decision 52 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
77d faster than avg
Panel avg: 129d · This submission: 52d
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 211
Devices cleared under the same product code (FYA) and FDA review panel - the closest regulatory comparables to K981073.
ROTECNO 2000 SURGICAL GOWN
K982059 · Encompass Group, LLC · Nov 1998
MEDINE DISPOSABLE STERILE ZONED IMPERVIOUS SURGICAL GOWNS
K982693 · Medline Industries, Inc. · Oct 1998
MICROCOOL SURGICAL GOWN
K981393 · Kimberly-Clark Corp. · Jul 1998
GOWN POLY REINFORCED LARGE(PRODUCT NO.900-522)/(REORDER NO. 0522)
K971920 · Customed, Inc. · Dec 1997
PROVISION SURGICAL HELMET SYSTEM
K972832 · Depuy, Inc. · Oct 1997
ULTRASOUND TRANSDUCER DRAPE
K970893 · Protek Medical Products, Inc. · Oct 1997