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P.R.G. PERCUTANEOUS REPLACEMENT GASTROSTOMY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900884
510(k) Type
Traditional
Applicant
APPLIED MEDICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent with Drug
Decision Date
7/2/1990
Days to Decision
126 days

P.R.G. PERCUTANEOUS REPLACEMENT GASTROSTOMY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K900884
510(k) Type
Traditional
Applicant
APPLIED MEDICAL TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent with Drug
Decision Date
7/2/1990
Days to Decision
126 days