Last synced on 27 May 2022 at 11:05 pm

MEDPULSE RESPIRATORY VEST SYSTEM, MODEL 1000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982889
510(k) Type
Traditional
Applicant
ELECTROMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1999
Days to Decision
288 days
Submission Type
Summary

MEDPULSE RESPIRATORY VEST SYSTEM, MODEL 1000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K982889
510(k) Type
Traditional
Applicant
ELECTROMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1999
Days to Decision
288 days
Submission Type
Summary