510(k) K760970
- Device
- FLORIO CPC BAND
- Applicant
- RICHARD'S MEDICAL EQUIP., INC.
- 510(k) number
- K760970
- Product code
- HWN
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1976-11-23
- Date received
- 1976-11-04
- Regulation
- 888.4540
- Classification name
- Instrument, Compression
- Medical specialty
- Orthopedic
- Review panel
- Orthopedic
- 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#
- 9611616
- 3005677016
- 9617297
- 3008583793
- 9616671
- 3012429289
- 3006943846
- 3011623994
- 3015383864
- 3019356409
- 1834379
- 3012120772
- 8040278
- 2031009
- 3009051471
- 9611827
- 3004369035
- 2183449
- 9611579
- 3015212339
- 1722824
- 1833824
- 3005751028
- 2134947
- 3017435639
- 3006846753
- 3009509485
- 3010235355
- 3005031160
- 1226544
- 1064129
- 3013011598
- 9680718
- 3014257776
- 2027754
- 3008850074
- 3009106092
- 3004641308
- 3009971621
- 3010123256
- 3005641619
- 1530390
- 3006783837
- 3007993775
- 1822565
- 1722511
- 1030489
- 3010646402
- 2031966
- 3004176895
- 1424434
- 3008773560
- 3006128100
- 1221763
- 3007810456
- 1219518
- 3000931034
- 3004001706
- 1833986
- 3010667733
- 3010097171
- 1836161
- 3002807315
- 3022159082
- 8010935
- 3042248499
- 2431224
- 1526439
- 3013875765
- 9611281
- 3015876273
- 8010405
- 1649379
- 3015516266
- 1219655
- 9611390
- 2027467
- 3016032497
- 3005739886
- 3009882675
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code HWN #
Legacy Summary#
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FDA Review#
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