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ABD VARISOFT STEERABLE GUIDE WIRE AND ABD VARISOFT GUIDE WIRE EXTENSION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981936
510(k) Type
Traditional
Applicant
ADVANCED BIOMEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/16/2000
Days to Decision
624 days
Submission Type
Statement

ABD VARISOFT STEERABLE GUIDE WIRE AND ABD VARISOFT GUIDE WIRE EXTENSION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981936
510(k) Type
Traditional
Applicant
ADVANCED BIOMEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/16/2000
Days to Decision
624 days
Submission Type
Statement