ERIKA EXTENSION SETS
FDA 510(k) clearance K810823 · decided 1981-04-17
Clearance details
- K-number
- K810823
- Device name
- ERIKA EXTENSION SETS
- Applicant
- Erika, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1981-03-24
- Decision date
- 1981-04-17
- Days to decision
- 24 days
- Clearance type
- Traditional
- Product code
- FJK
- Device class
- 2
- Regulation number
- 876.5820
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Walker, MI, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.