Last synced on 14 November 2025 at 11:06 pm

RESPIRATION MONITOR

Page Type
Cleared 510(K)
510(k) Number
K832999
510(k) Type
Traditional
Applicant
LITTON MEDICAL ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1984
Days to Decision
179 days

RESPIRATION MONITOR

Page Type
Cleared 510(K)
510(k) Number
K832999
510(k) Type
Traditional
Applicant
LITTON MEDICAL ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/1984
Days to Decision
179 days