T4/T5 Hytrel Togas

FDA 510(k) K121664 · Stryker Corporation

Substantially Equivalent

510(k) numberK121664

Submission

Device name
T4/T5 Hytrel Togas
Applicant
Stryker Corporation
Kalamazoo, MI, US
Received
June 5, 2012
Decision date
March 10, 2014
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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

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K253003Non-sterile Level 3 Surgical Gown (4025); Sterile Level 3 Surgical Gown (M4025)…FYA · Traditional Hubei Xinxin Non-Woven Co., Ltd.04/20/2026SE
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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

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Questions and answers

When was T4/T5 Hytrel Togas cleared by the FDA?

T4/T5 Hytrel Togas (K121664) received a 510(k) decision of Substantially Equivalent on March 10, 2014, 643 days after the submission was received.

What is the product code of K121664?

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