Last synced on 27 January 2023 at 11:04 pm

SILASTIC PERCUTANEOUS GASTROINTEST. TUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K760945
510(k) Type
Traditional
Applicant
DOW CORNING CORP. HEALTHCARE INDUSTRIES MATERIALS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/1976
Days to Decision
22 days