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HOLGRATH COMBINED SPINAL EPIDURAL NEEDLE SET

Page Type
Cleared 510(K)
510(k) Number
K954835
510(k) Type
Traditional
Applicant
HOLGRATH MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/1996
Days to Decision
103 days
Submission Type
Statement

HOLGRATH COMBINED SPINAL EPIDURAL NEEDLE SET

Page Type
Cleared 510(K)
510(k) Number
K954835
510(k) Type
Traditional
Applicant
HOLGRATH MEDICAL TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/31/1996
Days to Decision
103 days
Submission Type
Statement