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KESTREL LENS CASE 731H-893S/P-1700-2611

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900053
510(k) Type
Traditional
Applicant
KESTREL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1990
Days to Decision
27 days

KESTREL LENS CASE 731H-893S/P-1700-2611

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900053
510(k) Type
Traditional
Applicant
KESTREL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1990
Days to Decision
27 days