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BILICHEK NON-INVASIVE BILIRUBIN ANALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983071
510(k) Type
Traditional
Applicant
RESPIRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1999
Days to Decision
183 days
Submission Type
Statement

BILICHEK NON-INVASIVE BILIRUBIN ANALYZER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983071
510(k) Type
Traditional
Applicant
RESPIRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1999
Days to Decision
183 days
Submission Type
Statement