510(k) K823315
- Device
- DENTAL INSTRUMENTS - KNIVES
- Applicant
- MILTEX, INC.
- 510(k) number
- K823315
- Product code
- EJZ
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1982-11-24
- Date received
- 1982-11-08
- Regulation
- 872.4565
- Classification name
- Knife, Margin Finishing, Operative
- Medical specialty
- Dental
- Review panel
- Dental
- 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#
- 3014334038
- 2521453
- 3011371465
- 1416605
- 3014937043
- 8041151
- 2183301
- 3010864832
- 3009968482
- 1836161
- 3003969055
- 8010732
- 8040278
- 2511556
- 3008922120
- 3000219976
- 3035708926
- 9613083
- 5906
- 9681540
- 3010288346
- 9611283
- 3004193466
- 9613926
- 3012421607
- 1422507
- 9681748
- 2246990
- 3009171220
- 9611062
- 9680026
- 9616119
- 3003418325
- 3009340886
- 9610612
- 9611367
- 3016965929
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code EJZ #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K872622 | ORTHODONTIC ARCH | Wonder Wire | 1987-10-09 |
Legacy Summary#
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FDA Review#
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