510(k) K840907
- Device
- POST-AID
- Applicant
- E.W. Link, Inc.
- 510(k) number
- K840907
- Product code
- KCM
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1984-08-02
- Date received
- 1984-02-28
- Regulation
- 874.5220
- Classification name
- Dropper, Ent
- Medical specialty
- Ear, Nose, Throat
- Review panel
- Ear, Nose, Throat
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 9613926
- 3016734024
- 1419844
- 3008627763
- 3013188547
- 8021764
- 1218347
- 2183416
- 3039261408
- 3010595767
- 3016585381
- 1926681
- 8040278
- 3008650974
- 3003348846
- 3008338766
- 3013823570
- 3009881291
- 3012316249
- 1058602
- 2521373
Source Documents#
510(k) summary PDF not indicated by FDA