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MODIFICATION TO THE SITE PERISTALTIC MODULE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883199
510(k) Type
Traditional
Applicant
CHIRON VISION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/1988
Days to Decision
49 days

MODIFICATION TO THE SITE PERISTALTIC MODULE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883199
510(k) Type
Traditional
Applicant
CHIRON VISION CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/15/1988
Days to Decision
49 days