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ALDRETE EPIDURAL NEEDLE WITHOUT INTRODUCER

Page Type
Cleared 510(K)
510(k) Number
K972595
510(k) Type
Traditional
Applicant
AVID N.I.T., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/1998
Days to Decision
313 days
Submission Type
Statement

ALDRETE EPIDURAL NEEDLE WITHOUT INTRODUCER

Page Type
Cleared 510(K)
510(k) Number
K972595
510(k) Type
Traditional
Applicant
AVID N.I.T., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/20/1998
Days to Decision
313 days
Submission Type
Statement