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CROUCH CORNEAL PROTECTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K833256
510(k) Type
Traditional
Applicant
STAR INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1984
Days to Decision
141 days

CROUCH CORNEAL PROTECTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K833256
510(k) Type
Traditional
Applicant
STAR INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1984
Days to Decision
141 days