Last synced on 14 November 2025 at 11:06 pm

ARGYLE DUO-TUBE

Page Type
Cleared 510(K)
510(k) Number
K822631
510(k) Type
Traditional
Applicant
SHERWOOD MEDICAL CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/1982
Days to Decision
9 days

ARGYLE DUO-TUBE

Page Type
Cleared 510(K)
510(k) Number
K822631
510(k) Type
Traditional
Applicant
SHERWOOD MEDICAL CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/1982
Days to Decision
9 days