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LUMENCATH APPLICATOR SET, MODELS 189. 795, 189.796, 189.797, 189.798, LUMENCATH CATHETERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091598
510(k) Type
Special
Applicant
NUCLETRON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/29/2009
Days to Decision
26 days
Submission Type
Statement

LUMENCATH APPLICATOR SET, MODELS 189. 795, 189.796, 189.797, 189.798, LUMENCATH CATHETERS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091598
510(k) Type
Special
Applicant
NUCLETRON CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/29/2009
Days to Decision
26 days
Submission Type
Statement