CUMEVAC— 510(k) K874410
Substantially EquivalentCumes-Honikman Partnership
FDA 510(k) clearance K874410 for CUMEVAC, Substantially Equivalent on 1987-12-03. Applicant: Cumes-Honikman Partnership. Device class: 1.
Clearance details
- Applicant
- Cumes-Honikman Partnership
- Product code
- Code FFD
- Device class
- Class 1
- Regulation
- 21 CFR 876.4370
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Santa Barbara, CA, US
Recent devices under product code FFD
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