Last synced on 25 April 2025 at 11:05 pm

AXIOM-HVG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K955146
510(k) Type
Traditional
Applicant
AXIOM MANUFACTURING
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
5/17/1996
Days to Decision
186 days

AXIOM-HVG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K955146
510(k) Type
Traditional
Applicant
AXIOM MANUFACTURING
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
5/17/1996
Days to Decision
186 days