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MICRATOME MS7000 -ADVANCED CORNEAL/REFRACTIVE INSTRUMENTATION (ACRI)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981554
510(k) Type
Traditional
Applicant
MICRA INSTRUMENTS LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
12/22/1998
Days to Decision
235 days
Submission Type
Summary

MICRATOME MS7000 -ADVANCED CORNEAL/REFRACTIVE INSTRUMENTATION (ACRI)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981554
510(k) Type
Traditional
Applicant
MICRA INSTRUMENTS LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
12/22/1998
Days to Decision
235 days
Submission Type
Summary