ELECTRONIC STETHOSCOPE
FDA 510(k) clearance K761308 · decided 1977-01-06
Clearance details
- K-number
- K761308
- Device name
- ELECTRONIC STETHOSCOPE
- Applicant
- Medline Industries, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1976-12-23
- Decision date
- 1977-01-06
- Days to decision
- 14 days
- Clearance type
- Traditional
- Product code
- DPD
- Device class
- 2
- Regulation number
- 862.3320
- Medical specialty
- Clinical Toxicology
- Advisory committee
- Clinical Toxicology
- 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.