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MEGABEAM REUSABLE FIBER OPTIC HANDPIECE AND NEEDLES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980389
510(k) Type
Traditional
Applicant
Ceram Optec, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/1998
Days to Decision
177 days
Submission Type
Summary

MEGABEAM REUSABLE FIBER OPTIC HANDPIECE AND NEEDLES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980389
510(k) Type
Traditional
Applicant
Ceram Optec, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/1998
Days to Decision
177 days
Submission Type
Summary