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REFRACTEC MCS-100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980522
510(k) Type
Traditional
Applicant
REFRACTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
7/22/1998
Days to Decision
162 days
Submission Type
Statement

REFRACTEC MCS-100

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980522
510(k) Type
Traditional
Applicant
REFRACTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent - With Limitations
Decision Date
7/22/1998
Days to Decision
162 days
Submission Type
Statement