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AUGASTROENTEROLOGY-UROLOGY BIOPSY INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954231
510(k) Type
Traditional
Applicant
PROMEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/1995
Days to Decision
11 days
Submission Type
Statement

AUGASTROENTEROLOGY-UROLOGY BIOPSY INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K954231
510(k) Type
Traditional
Applicant
PROMEX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/1995
Days to Decision
11 days
Submission Type
Statement