ARGYLE MEDIASTINAL DRAIN— 510(k) K822318
Substantially EquivalentSherwood Medical Co.
FDA 510(k) clearance K822318 for ARGYLE MEDIASTINAL DRAIN, Substantially Equivalent on 1982-08-27. Applicant: Sherwood Medical Co.. Device class: 1.
Clearance details
- Applicant
- Sherwood Medical Co.
- Product code
- Code GBS
- Device class
- Class 1
- Regulation
- 21 CFR 878.4200
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.