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HOLGRATH PLASTIC-HUB EPIDURAL NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K944906
510(k) Type
Traditional
Applicant
HOLGRATH MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/1995
Days to Decision
245 days
Submission Type
Statement

HOLGRATH PLASTIC-HUB EPIDURAL NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K944906
510(k) Type
Traditional
Applicant
HOLGRATH MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/7/1995
Days to Decision
245 days
Submission Type
Statement