VIVONEX MASS GASTRASTOMY TUBE
FDA 510(k) clearance K822516 · decided 1982-09-07
Clearance details
- K-number
- K822516
- Device name
- VIVONEX MASS GASTRASTOMY TUBE
- Applicant
- Norwich Eaton Pharmaceuticals, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1982-08-20
- Decision date
- 1982-09-07
- Days to decision
- 18 days
- Clearance type
- Traditional
- Product code
- KHT
- Device class
- 1
- Regulation number
- 866.5370
- Medical specialty
- Immunology
- Advisory committee
- Immunology
- 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.