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RECTOSIGHT RS300-04;AND PROTOSIGHT PS300-04 DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011825
510(k) Type
Special
Applicant
SIGHTLINE TECHNOLOGIES LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
7/11/2001
Days to Decision
30 days
Submission Type
Statement

RECTOSIGHT RS300-04;AND PROTOSIGHT PS300-04 DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011825
510(k) Type
Special
Applicant
SIGHTLINE TECHNOLOGIES LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
7/11/2001
Days to Decision
30 days
Submission Type
Statement