BECKMAN ADENOID CURRETTE
FDA 510(k) clearance K822189 · decided 1982-08-16
Clearance details
- K-number
- K822189
- Device name
- BECKMAN ADENOID CURRETTE
- Applicant
- Kelleher Corp.
- Decision
- Substantially Equivalent
- Date received
- 1982-07-23
- Decision date
- 1982-08-16
- Days to decision
- 24 days
- Clearance type
- Traditional
- Product code
- KBJ
- Device class
- 1
- Regulation number
- 874.4420
- Medical specialty
- Ear, Nose, Throat
- Advisory committee
- Ear, Nose, Throat
- 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.