ELECTRONIC STETHOSCOPE— 510(k) K761308
Substantially EquivalentMedline Industries, Inc.
FDA 510(k) clearance K761308 for ELECTRONIC STETHOSCOPE, Substantially Equivalent on 1977-01-06. Applicant: Medline Industries, Inc.. Device class: 2.
Clearance details
- Applicant
- Medline Industries, Inc.
- Product code
- Code DPD
- Device class
- Class 2
- Regulation
- 21 CFR 862.3320
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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