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NEWPORT HT50 VENTILATOR WITH HUMIDIFIER HT50-H, NEWPORT HT50 VENTILATOR WITHOUT HUMIDIFIER, HT50-H1, NEWPORT HT50 VENTIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992133
510(k) Type
Traditional
Applicant
NEWPORT MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
8/4/2000
Days to Decision
408 days

NEWPORT HT50 VENTILATOR WITH HUMIDIFIER HT50-H, NEWPORT HT50 VENTILATOR WITHOUT HUMIDIFIER, HT50-H1, NEWPORT HT50 VENTIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992133
510(k) Type
Traditional
Applicant
NEWPORT MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
8/4/2000
Days to Decision
408 days