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HEAD HOLDING DEVICE/SLEEP APNEA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884493
510(k) Type
Traditional
Applicant
X-RAY SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/1989
Days to Decision
78 days

HEAD HOLDING DEVICE/SLEEP APNEA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884493
510(k) Type
Traditional
Applicant
X-RAY SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/12/1989
Days to Decision
78 days