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LOPER CELIAC PLEXUS BLOCK CATHETER KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895955
510(k) Type
Traditional
Applicant
OPTICON MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/1990
Days to Decision
134 days

LOPER CELIAC PLEXUS BLOCK CATHETER KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K895955
510(k) Type
Traditional
Applicant
OPTICON MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/22/1990
Days to Decision
134 days