Last synced on 23 September 2022 at 11:05 pm

CONTAIN X-RAY DETECTABLE LAP SPONGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K801768
510(k) Type
Traditional
Applicant
THE BUCKEYE CELLULOSE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/1980
Days to Decision
23 days

CONTAIN X-RAY DETECTABLE LAP SPONGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K801768
510(k) Type
Traditional
Applicant
THE BUCKEYE CELLULOSE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/1980
Days to Decision
23 days