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MONOJECT TUOHY POINT EPIDURAL NEEDLE (22G X 3 1/2)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951411
510(k) Type
Traditional
Applicant
SHERWOOD MEDICAL CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/1995
Days to Decision
34 days
Submission Type
Summary

MONOJECT TUOHY POINT EPIDURAL NEEDLE (22G X 3 1/2)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K951411
510(k) Type
Traditional
Applicant
SHERWOOD MEDICAL CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/1995
Days to Decision
34 days
Submission Type
Summary