Last synced on 14 November 2025 at 11:06 pm

RECTAL & HARRIS FLUSH TUBES

Page Type
Cleared 510(K)
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

RECTAL & HARRIS FLUSH TUBES

Page Type
Cleared 510(K)
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