Last synced on 9 May 2025 at 11:05 pm

TOTAL CROSS .021 PERCUT. TRANSLUMINAL ANGIO. CATH.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921856
510(k) Type
Traditional
Applicant
SCHNEIDER INTL., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/1992
Days to Decision
95 days
Submission Type
Statement

TOTAL CROSS .021 PERCUT. TRANSLUMINAL ANGIO. CATH.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921856
510(k) Type
Traditional
Applicant
SCHNEIDER INTL., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/21/1992
Days to Decision
95 days
Submission Type
Statement