Last synced on 4 February 2023 at 10:33 pm

HC1000P SLEEP DIAGNOSIS SOFTWARE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073269
510(k) Type
Traditional
Applicant
HYPNOCORE, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2008
Days to Decision
149 days
Submission Type
Summary

HC1000P SLEEP DIAGNOSIS SOFTWARE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K073269
510(k) Type
Traditional
Applicant
HYPNOCORE, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/18/2008
Days to Decision
149 days
Submission Type
Summary