510(k) K801975
- Device
- Little Giant I & Ii Handpiece Control
- Applicant
- SILVERMAN'S
- 510(k) number
- K801975
- Product code
- EIA
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1980-09-09
- Date received
- 1980-08-19
- Regulation
- 872.6640
- Classification name
- Unit, Operative Dental
- 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#
- 3000190675
- 3038718579
- 1226003
- 3013237609
- 3003548115
- 9680845
- 9614446
- 3015967359
- 3003855981
- 9610617
- 3009774128
- 3006113289
- 1722638
- 2081055
- 2023950
- 1054713
- 3010373494
- 3007962015
- 3019103
- 1824362
- 3002819275
- 3003136642
- 1523530
- 3010141593
- 3013734432
- 2648666
- 3010707607
- 8044015
- 1062917
- 3003188647
- 3004884150
- 8030876
- 3008559238
- 3011326671
- 3017604
- 3015376465
- 3042256511
- 3011300255
- 3000219976
- 3003637274
- 3021551875
- 1018470
- 3030089804
- 3012421607
- 3006946348
- 3030126955
- 3007997036
- 3004082121
- 3022226
- 8044167
- 1017522
- 3010446656
- 3033509898
- 3015980207
- 1649995
- 9614977
- 3008344699
- 2520265
- 3009797758
- 3039246551
- 2020475
- 3010939897
- 3003917473
- 3004064895
- 3002564560
- 3010202439
- 9681829
- 3005938413
- 9681479
- 9710613
- 3007518359
- 8040233
- 8020994
- 2916440
- 3029780
- 3002807636
- 3008813313
- 3014980444
- 1319130
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code EIA#
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