510(k) K821682
- Device
- TRUNCAL ORTHOSIS
- Applicant
- SURGICAL APPLIANCE INDUSTRIES, INC.
- 510(k) number
- K821682
- Product code
- IQE
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1982-06-24
- Date received
- 1982-06-08
- Regulation
- 890.3490
- Classification name
- Orthosis, Lumbar
- Medical specialty
- Physical Medicine
- Review panel
- Physical Medicine
- 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#
- 3005597706
- 3010220099
- 2182345
- 3015727296
- 3043729627
- 3016872092
- 3006619688
- 3027328721
- 3021244152
- 3001917653
- 3013375723
- 3010239526
- 1812798
- 1063727
- 3010785927
- 3008247697
- 3015069144
- 3010097863
- 3008008970
- 3013180212
- 3010729057
- 3010694026
- 3013957847
- 3003764610
- 3008903689
- 3017264244
- 3007305128
- 3010961310
- 3011678115
- 3021630959
- 3003895865
- 3005841961
- 3014947080
- 3007615436
- 9616086
- 1054236
- 9616933
- 3045853560
- 3031595580
- 3008216220
- 3009759525
- 1058152
- 3014204631
- 3010960892
- 1037964
- 1417592
- 3013527364
- 3012951155
- 3005282622
- 3016758972
- 3010894302
- 9617759
- 9680104
- 3008523132
- 3012027699
- 3014144875
- 3023212654
- 3011786430
- 3014204518
- 3030446844
- 3004096515
- 1641302
- 1511629
- 3007207474
- 3014560743
- 3017926429
- 3014658541
- 1422443
- 3013770567
- 3009437400
- 3017202421
- 3042227943
- 3011120089
- 3011689956
- 3016964847
- 3011287176
- 3014345255
- 3003884600
- 3012453117
- 3015134013
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code IQE #
Legacy Summary#
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FDA Review#
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