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NEUROTHERM RF CANNULA

Page Type
Cleared 510(K)
510(k) Number
K994344
510(k) Type
Traditional
Applicant
ROCKET MEDICAL PLC
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/21/2000
Days to Decision
90 days
Submission Type
Summary

NEUROTHERM RF CANNULA

Page Type
Cleared 510(K)
510(k) Number
K994344
510(k) Type
Traditional
Applicant
ROCKET MEDICAL PLC
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/21/2000
Days to Decision
90 days
Submission Type
Summary