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NTECH CYSTOSCOPES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980592
510(k) Type
Traditional
Applicant
N-Tech Endoscopy, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/1998
Days to Decision
70 days
Submission Type
Summary

NTECH CYSTOSCOPES

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980592
510(k) Type
Traditional
Applicant
N-Tech Endoscopy, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/1998
Days to Decision
70 days
Submission Type
Summary