Last synced on 27 January 2023 at 11:04 pm

KERATOME BLADE (135 MICRON, MODEL 300135), (160 MICRON, MODEL 300160), (200 MICRON, MODEL 30020)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980510
510(k) Type
Traditional
Applicant
MICROSPECIALTIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/1998
Days to Decision
80 days
Submission Type
Summary

KERATOME BLADE (135 MICRON, MODEL 300135), (160 MICRON, MODEL 300160), (200 MICRON, MODEL 30020)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980510
510(k) Type
Traditional
Applicant
MICROSPECIALTIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/1998
Days to Decision
80 days
Submission Type
Summary