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XENON 300MX

Page Type
Cleared 510(K)
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)
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