510(k) K770349
- Device
- RIGID TEACHING ATTACHMENT
- Applicant
- Richard Wolf Medical Instruments Corp.
- 510(k) number
- K770349
- Product code
- HWN
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-03-07
- Date received
- 1977-02-22
- Regulation
- 888.4540
- Classification name
- Instrument, Compression
- Medical specialty
- Orthopedic
- Review panel
- Orthopedic
- 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#
- 3008850074
- 8010944
- 9614093
- 3008773560
- 3006128100
- 8010379
- 3006563559
- 2183449
- 9610612
- 3008650117
- 1219518
- 3025114181
- 3039169546
- 9611579
- 3017435639
- 9611616
- 3019356409
- 3010287737
- 3033509898
- 9680518
- 3010303097
- 3014938863
- 3007993775
- 3005067367
- 1530390
- 8010935
- 3009971621
- 3018094310
- 1421101
- 9680059
- 1833824
- 3004371426
- 3009158523
- 3007410669
- 3013875765
- 1424434
- 3010097171
- 3004001706
- 3009790163
- 3010509633
- 2031966
- 3010363503
- 3012429289
- 3031261833
- 9616671
- 1824199
- 9611827
- 1526439
- 1818910
- 9617155
- 3006460162
- 3005061536
- 3042248499
- 3008812560
- 3008583793
- 3009882675
- 3006783837
- 3005031160
- 3009417901
- 3015440604
- 3005677016
- 3004983210
- 1720747
- 1825034
- 1064129
- 3012120772
- 3009380063
- 8030607
- 1226544
- 1833986
- 3003407244
- 3006639944
- 3005641619
- 1828288
- 8043862
- 2134947
- 3007728266
- 1822565
- 3010536692
- 3025603301
Source Documents#
510(k) summary PDF not indicated by FDA