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TUOHY EPIDURAL NEEDLES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961152
510(k) Type
Traditional
Applicant
HAKKO SHOJI CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/1997
Days to Decision
362 days
Submission Type
Statement

TUOHY EPIDURAL NEEDLES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961152
510(k) Type
Traditional
Applicant
HAKKO SHOJI CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/1997
Days to Decision
362 days
Submission Type
Statement