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ST-302 INFRAREX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990233
510(k) Type
Traditional
Applicant
Skylark Device Co., Ltd.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
10/27/1999
Days to Decision
275 days
Submission Type
Statement

ST-302 INFRAREX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990233
510(k) Type
Traditional
Applicant
Skylark Device Co., Ltd.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
10/27/1999
Days to Decision
275 days
Submission Type
Statement