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MOD. ENDONEEDLE SINGLE-USE PNEUMOPERITONEUM NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860102
510(k) Type
Traditional
Applicant
ENDOTHERAPEUTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1986
Days to Decision
33 days

MOD. ENDONEEDLE SINGLE-USE PNEUMOPERITONEUM NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K860102
510(k) Type
Traditional
Applicant
ENDOTHERAPEUTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1986
Days to Decision
33 days