SPARTA BRONCHIAL BRUSH
FDA 510(k) clearance K781365 · decided 1978-08-14
Clearance details
- K-number
- K781365
- Device name
- SPARTA BRONCHIAL BRUSH
- Applicant
- Sparta Instrument Corp.
- Decision
- Substantially Equivalent
- Date received
- 1978-08-07
- Decision date
- 1978-08-14
- Days to decision
- 7 days
- Clearance type
- Traditional
- Product code
- KTI
- Device class
- 2
- Regulation number
- 874.4680
- Medical specialty
- Ear, Nose, Throat
- Advisory committee
- Ear, Nose, Throat
- 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.