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EPIDURAL NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K980536
510(k) Type
Traditional
Applicant
MANAN MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/1998
Days to Decision
170 days
Submission Type
Statement

EPIDURAL NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K980536
510(k) Type
Traditional
Applicant
MANAN MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/1998
Days to Decision
170 days
Submission Type
Statement