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HOLGRATH COMBINED SPINAL EPIDURAL NEEDLE SET

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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