Cool-Zone

FDA 510(k) K963809 · Kappler USA

Substantially Equivalent

510(k) numberK963809

Submission

Device name
Cool-Zone
Applicant
Kappler USA
Guntersville, AL, US
Received
September 23, 1996
Decision date
November 20, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FYA – Gown, Surgical
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4040
Specialty
General, Plastic Surgery

Other 510(k)s with product code FYA

510(k)DeviceApplicantDecision
K260407Principle & Will ANSI/AAMI PB 70 (Sterile/Non-sterile) Level 3 Surgical Gowns…FYA · Traditional Principle & Will Co., Ltd.08/26/2026SE
K261028Surgical Gown Level2 (S, M, L, XL, XXL, XXXL)FYA · Traditional Yadu Medical (Henan) Co., Ltd.08/07/2026SE
K261949NYES Tuff Cuff L3 Disposable GownsFYA · Special New York Embroidery Studio07/10/2026SE
K252575Tuff Cuff™ Disposable Surgical Gowns AAMI L4 Sterile-Large (ML-L4-STL-DC-L)FYA · Traditional New York Embroidery Studio (NYES)06/04/2026SE
K260725BAÜMER Surgical Gowns (COP01, COP04, COP05, COP10)FYA · Traditional Hindernis DE Mexico, S.A.P.I. DE C.V.05/12/2026SE
K253243Cardinal Health™ Poly Reinforced Surgical GownFYA · Abbreviated Cardinal Health 200, LLC04/28/2026SE
K253003Non-sterile Level 3 Surgical Gown (4025); Sterile Level 3 Surgical Gown (M4025)…FYA · Traditional Hubei Xinxin Non-Woven Co., Ltd.04/20/2026SE
K251860Copioumed AAMI 3 Surgical GownFYA · Traditional Copioumed International, Inc.02/26/2026SE
K252301Henan Yadu Level 4 Surgical Gowns (Reinforced)FYA · Traditional Yadu Medical (Henan) Co., Ltd.02/04/2026SE
K250564Surgical Gown (Level 3: S, M, L, XL, XXL, XXXL)FYA · Traditional Yadu Medical (Henan) Co., Ltd.12/03/2025SE

More from Yadu Medical (Henan) Co., Ltd.

510(k)DeviceDecision
K992445Med-Guard Surgeon's GownFYA · Traditional 02/18/2000SE

Questions and answers

When was Cool-Zone cleared by the FDA?

Cool-Zone (K963809) received a 510(k) decision of Substantially Equivalent on November 20, 1996, 58 days after the submission was received.

What is the product code of K963809?

The FDA product code is FYA – Gown, Surgical, a Class II (moderate risk) device regulated under 21 CFR 878.4040.