AXIOM FEEDING GASTRO TUBE
FDA 510(k) clearance K831823 · decided 1983-08-12
Clearance details
- K-number
- K831823
- Device name
- AXIOM FEEDING GASTRO TUBE
- Applicant
- Axiom Medical, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1983-06-07
- Decision date
- 1983-08-12
- Days to decision
- 66 days
- Clearance type
- Traditional
- Product code
- KNT
- Device class
- 2
- Regulation number
- 876.5980
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
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Recalls involving this device
No recalls on record reference this clearance.