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AHIP INTERNAL TRIGGER POINT WAND MODEL: 1

Page Type
Cleared 510(K)
PDF
Full PDF / Letter
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN100023
510(k) Type
Post-NSE
Applicant
National Center For Pelvic Pain Research Devices,
Country
United States
FDA Decision
Deleted
Decision Date
11/20/2012
Days to Decision
823 days

AHIP INTERNAL TRIGGER POINT WAND MODEL: 1

Page Type
Cleared 510(K)
PDF
Full PDF / Letter
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN100023
510(k) Type
Post-NSE
Applicant
National Center For Pelvic Pain Research Devices,
Country
United States
FDA Decision
Deleted
Decision Date
11/20/2012
Days to Decision
823 days