510(k) K781098
- Device
- Brush, Applicator
- Applicant
- 3M COMPANY
- 510(k) number
- K781098
- Product code
- KXR
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1978-09-29
- Date received
- 1978-07-03
- Regulation
- 872.3140
- Classification name
- Applicator, Resin
- Medical specialty
- Dental
- Review panel
- Dental
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 8124 Pacific Ave. White City OR US 97503 97503
FDA Registration Numbers#
- 3007255375
- 9680887
- 3038718579
- 9611385
- 3004425647
- 2523320
- 1215305
- 2024980
- 9680845
- 3005176727
- 3036269993
- 3005558160
- 3016447764
- 3017910185
- 2511556
- 8040278
- 2023950
- 8010638
- 3007284437
- 3025307990
- 3018047916
- 3031582434
- 1051594
- 3002808149
- 3007210751
- 3007167099
- 2437780
- 3010598169
- 3006264569
- 3002675176
- 3026760
- 3003120666
- 1815540
- 3004475754
- 8044164
- 3003694926
- 3011824442
- 3012477813
- 1937100
- 2241860
- 3035693034
- 3012421607
- 3003621174
- 3006694515
- 3011526299
- 3010931810
- 2086043
- 3003449480
- 2916735
- 1281412
- 3011279497
- 3042272797
- 1718476
- 1718912
- 3013271380
- 1420089
- 2081322
- 3013557697
- 3027234828
- 2183301
- 3009420946
- 2133714
- 3017498782
- 9612352
- 3011707926
- 3014683120
- 3013508670
- 3031841433
- 3038632739
- 3002807420
- 3003491259
- 3004966444
- 2431069
- 3042244574
- 3015272949
- 1450653
- 3009171220
- 9613079
- 3009496224
Source Documents#
510(k) summary PDF not indicated by FDA