BRIOX MODEL 2000-CQ QUIET COMPRESSOR
FDA 510(k) clearance K791238 · decided 1979-07-24
Clearance details
- K-number
- K791238
- Device name
- BRIOX MODEL 2000-CQ QUIET COMPRESSOR
- Applicant
- Briox Technologies, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1979-07-06
- Decision date
- 1979-07-24
- Days to decision
- 18 days
- Clearance type
- Traditional
- Product code
- JCX
- Device class
- 2
- Regulation number
- 878.4780
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- 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.