Atlas FDA

PolyWear® Personal Protective Level 3 Gown

FDA 510(k) clearance K230384 · decided 2023-08-11

Clearance details

K-number
K230384
Device name
PolyWear® Personal Protective Level 3 Gown
Applicant
PolyConversions, Inc.
Decision
Substantially Equivalent
Date received
2023-02-14
Decision date
2023-08-11
Days to decision
178 days
Clearance type
Traditional
Product code
QPC
Device class
2
Regulation number
878.4040
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Champaign, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
VR® Personal Protective Level 3 Gown (VR Gowns) (K252940)PolyConversions, Inc.2025-12-16
AAMI Level 4 Protective; Gown (K242689)Azac Group2025-01-13
Medline Open-back Level 3 Protective Gown (K233526)Medline Industries, LP2024-03-05
Protective Gown AAMI Level 4 (K222128)Kenpax International Limited2023-08-08
Dukal Corporation AAMI Level 4 Open-Back Protective Gown (K212464)Dukal Corporation2022-03-30
Donagamex Blue Performance Protective Gown (K203821)Dong Nai Garment Corporation (Donagamex)2021-12-17
ProTEC-USA EZDoff Gown (K210405)Cadillac Products, Inc.2021-12-15
Cardinal HealthTM Poly-Coated Open-Back Protective Gown (K182830)Cardinal Health200, LLC2019-04-26
Safecare Open Back Protective Gowns and ValueCare Open Back Protective Gowns (K160337)Bam Corporation Limited2017-07-07

Recalls involving this device

No recalls on record reference this clearance.