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HAYEK OSCILLATOR, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K921726
510(k) Type
Traditional
Applicant
RESPIRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/1992
Days to Decision
15 days
Submission Type
Statement

HAYEK OSCILLATOR, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K921726
510(k) Type
Traditional
Applicant
RESPIRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/1992
Days to Decision
15 days
Submission Type
Statement