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PULSE KLYSTRON AMPLIFIER (L-5822-00)

Page Type
Cleared 510(K)
510(k) Number
K951142
510(k) Type
Traditional
Applicant
LITTON SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/1995
Days to Decision
95 days
Submission Type
Summary

PULSE KLYSTRON AMPLIFIER (L-5822-00)

Page Type
Cleared 510(K)
510(k) Number
K951142
510(k) Type
Traditional
Applicant
LITTON SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/1995
Days to Decision
95 days
Submission Type
Summary