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PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K885220
510(k) Type
Traditional
Applicant
ETHOX CORP.
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
9/25/1989
Days to Decision
279 days