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FDA 510(k) Applications Submitted by Sturdy Industrial Co., Ltd
FDA 510(k) Number
Submission Date
Device Name
Applicant
K032596
08/22/2003
STURDY MANUAL RESUSCITATOR
STURDY INDUSTRIAL CO., LTD
K231489
05/23/2023
Sturdy Autoclave Super Microm
Sturdy Industrial Co., Ltd
K181993
07/26/2018
STURDY Autoclave Super Microm (models SA-260MA and SA-260MA-R)
Sturdy Industrial Co., Ltd
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