MP-500 ELECTRONIC NEBULIZER— 510(k) K862171
Substantially EquivalentThe Timeter Group
FDA 510(k) clearance K862171 for MP-500 ELECTRONIC NEBULIZER, Substantially Equivalent on 1986-07-14. Applicant: The Timeter Group. Device class: 1.
Clearance details
- Applicant
- The Timeter Group
- Product code
- Code KFZ
- Device class
- Class 1
- Regulation
- 21 CFR 868.5460
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lancaster, PA, US
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