DREAM CATCHER— 510(k) K972122
Substantially EquivalentRest Technologies, Inc.
FDA 510(k) clearance K972122 for DREAM CATCHER, Substantially Equivalent on 1997-08-29. Applicant: Rest Technologies, Inc.. Device class: 2.
Clearance details
- Applicant
- Rest Technologies, Inc.
- Product code
- Code GXY
- Device class
- Class 2
- Regulation
- 21 CFR 882.1320
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Santa Monica, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.