POST-AID
FDA 510(k) clearance K840907 · decided 1984-08-02
Clearance details
- K-number
- K840907
- Device name
- POST-AID
- Applicant
- E.W. Link, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1984-02-28
- Decision date
- 1984-08-02
- Days to decision
- 156 days
- Clearance type
- Traditional
- Product code
- KCM
- Device class
- 1
- Regulation number
- 874.5220
- 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.