Last synced on 25 January 2026 at 3:41 am

SECCA TUBULAR ELECTRODE DEVICE, MODEL A4000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000170
510(k) Type
Special
Applicant
Conway Stuart Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2000
Days to Decision
27 days
Submission Type
Statement

SECCA TUBULAR ELECTRODE DEVICE, MODEL A4000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K000170
510(k) Type
Special
Applicant
Conway Stuart Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/2000
Days to Decision
27 days
Submission Type
Statement