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TUOHY EPIDURAL NEEDLES

Page Type
Cleared 510(K)
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)
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