RESPISOMNOGRAPH— 510(k) K861326
Substantially EquivalentDickstein, Shapiro & Morin
FDA 510(k) clearance K861326 for RESPISOMNOGRAPH, Substantially Equivalent on 1986-06-13. Applicant: Dickstein, Shapiro & Morin. Device class: 2.
Clearance details
- Applicant
- Dickstein, Shapiro & Morin
- Product code
- Code BZQ
- Device class
- Class 2
- Regulation
- 21 CFR 868.2375
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
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