MAXI-MISER HUMIDIFIER INSERT 1020
FDA 510(k) clearance K841569 · decided 1984-05-30
Clearance details
- K-number
- K841569
- Device name
- MAXI-MISER HUMIDIFIER INSERT 1020
- Applicant
- Nova-Ventrx
- Decision
- Substantially Equivalent
- Date received
- 1984-04-17
- Decision date
- 1984-05-30
- Days to decision
- 43 days
- Clearance type
- Traditional
- Advisory committee
- Unknown
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.