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RECTAL & HARRIS FLUSH TUBES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K800510
510(k) Type
Traditional
Applicant
MEDI-CRAFT LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/8/1980
Days to Decision
35 days