510(k) K060298
- Device
- PILL PHONE
- Applicant
- VOCEL
- 510(k) number
- K060298
- Product code
- NXQ
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2006-03-29
- Date received
- 2006-02-06
- Regulation
- 890.5050
- Classification name
- Reminder, Medication
- Medical specialty
- Physical Medicine
- Review panel
- General Hospital
- Device class
- 1
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- No
Applicant Contact#
- Contact
- KEITH A BARRITT
- Address
- 1425 K St., NW, Suite 1100 Washington DC US 20005 20005
FDA Registration Numbers#
- 3019102046
- 9710514
- 3012314549
- 3023272766
- 3007729562
- 3017417635
- 3027315347
- 3007499349
- 3012974595
- 3005951403
- 3010759878
- 3013400546
- 3013427569
- 3015729112
- 3043149893
- 3027557334
- 3011617226
- 1929691
- 3004485927
- 3020895410
- 2183416
- 3012933969
- 9616674
- 8010690
- 3014384423
- 3025664693
- 3025763866
- 3008770957
- 3014264913
- 3016851845
- 3016450032
- 3034365412
- 3009124884
- 3007200970
- 3015500804
- 3008997160
- 3011196543
- 3015745029
- 3032027298
- 3045010489
- 3011581939
- 3020530637
- 3017520312
- 3005569927
- 3008264111
- 3017026146
- 3017014798
- 3000126629
- 3009627223
- 3043041683
- 3015142815
- 3015316279
- 3021529075
- 3009155756
- 3008808082
- 3021542639
- 3042248397
- 3029917352
Source Documents#
Other 510(k) Records For Product Code NXQ #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K103009 | SENTICARE PILLSTATION | Senticare, Inc. | 2011-01-28 |
Legacy Summary#
summary
FDA Review#
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