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BARRON MICROKERATOME SYSTEM, MODEL B2000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983317
510(k) Type
Traditional
Applicant
BARRON PRECISION INSTRUMENTS, L.L.C.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/1998
Days to Decision
72 days
Submission Type
Summary

BARRON MICROKERATOME SYSTEM, MODEL B2000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983317
510(k) Type
Traditional
Applicant
BARRON PRECISION INSTRUMENTS, L.L.C.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/1998
Days to Decision
72 days
Submission Type
Summary