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PHX TECHNOLOGIES CORP., 10 MM THORACOSCOPY SCRAPPER DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K934280
510(k) Type
Traditional
Applicant
PHX TECHNOLOGIES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/13/1994
Days to Decision
135 days
Submission Type
Statement