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AMNICATHDL(TM) DT-IUPC2 DUAL LUMEN TRANS. TIPPED

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896122
510(k) Type
Traditional
Applicant
SPECTRAMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/1990
Days to Decision
87 days

AMNICATHDL(TM) DT-IUPC2 DUAL LUMEN TRANS. TIPPED

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896122
510(k) Type
Traditional
Applicant
SPECTRAMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/1990
Days to Decision
87 days