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CLEAR VINYL MONITORING CONNECTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K823340
510(k) Type
Traditional
Applicant
VERTEX MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/1982
Days to Decision
52 days

CLEAR VINYL MONITORING CONNECTOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K823340
510(k) Type
Traditional
Applicant
VERTEX MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/1982
Days to Decision
52 days