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CROSSVENT-4 VENTILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942938
510(k) Type
Traditional
Applicant
BIO-MED DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
9/19/1995
Days to Decision
454 days
Submission Type
Statement

CROSSVENT-4 VENTILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K942938
510(k) Type
Traditional
Applicant
BIO-MED DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent - Subject to Tracking Regulation
Decision Date
9/19/1995
Days to Decision
454 days
Submission Type
Statement