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XENON 300MX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980044
510(k) Type
Traditional
Applicant
PERKINELMER OPTOELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/1998
Days to Decision
87 days
Submission Type
Summary

XENON 300MX

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K980044
510(k) Type
Traditional
Applicant
PERKINELMER OPTOELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/1998
Days to Decision
87 days
Submission Type
Summary