Last synced on 25 November 2022 at 11:04 pm

MICRO-6-SERIES (MR-6, MR-6L) URETEROSCOPES, MRO-6 SERIES (MR-633, MR-642) URETEROSCOPES, MRO-7 SERIES (MRO-733) URETEROS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011849
510(k) Type
Traditional
Applicant
CIRCON VIDEO
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2001
Days to Decision
180 days
Submission Type
Statement

MICRO-6-SERIES (MR-6, MR-6L) URETEROSCOPES, MRO-6 SERIES (MR-633, MR-642) URETEROSCOPES, MRO-7 SERIES (MRO-733) URETEROS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011849
510(k) Type
Traditional
Applicant
CIRCON VIDEO
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/2001
Days to Decision
180 days
Submission Type
Statement