510(k) K770407
- Device
- SHIELD, DENTAL X-RAY, PROTECTIVE
- Applicant
- Worldwide Dental, Inc.
- 510(k) number
- K770407
- Product code
- IWO
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-03-15
- Date received
- 1977-03-04
- Regulation
- 892.6500
- Classification name
- Apron, Protective
- Medical specialty
- Radiology
- Review panel
- Radiology
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- N
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 2183301
- 3007791604
- 3006535976
- 3004980986
- 3017158347
- 3045058049
- 3020118
- 3031184338
- 3037040712
- 3016649599
- 3002532594
- 2431224
- 1218386
- 3008381089
- 3004168759
- 3015058854
- 3009222501
- 3011529314
- 3014314985
- 3005176727
- 3010198795
- 3034669683
- 3017299798
- 3016758972
- 3013269506
- 3034629649
- 3011434305
- 9680506
- 3014610488
- 3009233038
- 3016704566
- 3010864832
- 3016968725
- 3017952343
- 3016766901
- 3006210673
- 3024088964
- 3008352964
- 3027815
- 3026030534
- 3010374972
- 3014819517
- 3011344631
- 3016733683
- 3023265420
- 2433012
- 3008496560
- 3007369190
- 3016171961
- 1053541
- 3043648115
- 3018269545
- 3038632739
- 3013846070
- 3017385563
- 3005257704
- 3033011342
- 3008062466
- 1063300
- 1222742
- 3007479164
- 3010147274
- 3005621808
- 3006897996
- 1834183
- 3017103765
- 3015384814
- 3011526299
- 9680934
- 9616872
- 3016452400
- 1219113
- 3007069733
- 2024312
- 2024351
- 3038282968
- 3003965134
- 9680411
- 3025001668
- 3015416207
Source Documents#
510(k) summary PDF not indicated by FDA