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PINNACLE R/O OR REDIFOCUS INTRODUCER R/O (COMPRISED OF A SHEATH & DILATOR)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984260
510(k) Type
Special
Applicant
TERUMO MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1999
Days to Decision
62 days
Submission Type
Summary

PINNACLE R/O OR REDIFOCUS INTRODUCER R/O (COMPRISED OF A SHEATH & DILATOR)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984260
510(k) Type
Special
Applicant
TERUMO MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1999
Days to Decision
62 days
Submission Type
Summary