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CIRCON ACMI BICAP HEMORRHOID SYSTEM BH-10 & BHP-20

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884252
510(k) Type
Traditional
Applicant
CIRCON ACMI
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1989
Days to Decision
91 days

CIRCON ACMI BICAP HEMORRHOID SYSTEM BH-10 & BHP-20

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884252
510(k) Type
Traditional
Applicant
CIRCON ACMI
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/1989
Days to Decision
91 days