SOFT EAR STETHOSCOPE
FDA 510(k) clearance K870600 · decided 1987-03-19
Clearance details
- K-number
- K870600
- Device name
- SOFT EAR STETHOSCOPE
- Applicant
- Kalajian Ent.
- Decision
- Substantially Equivalent
- Date received
- 1987-02-10
- Decision date
- 1987-03-19
- Days to decision
- 37 days
- Clearance type
- Traditional
- Product code
- CBG
- Device class
- 1
- Regulation number
- 868.5760
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- Location
- Chapel Hill, NC, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.