Last synced on 2 June 2023 at 11:04 pm

ENDOSCOPIC SCLEROTHERAPY BALLOON

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K821999
510(k) Type
Traditional
Applicant
RETECH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/1982
Days to Decision
51 days

ENDOSCOPIC SCLEROTHERAPY BALLOON

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K821999
510(k) Type
Traditional
Applicant
RETECH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/27/1982
Days to Decision
51 days