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#
- 8010507
- 3012907824
- 2249769
- 3011789046
- 3009303371
- 3008364966
- 3009657307
- 3016096133
- 3030539818
- 3008048783
- 2182345
- 3005031124
- 3016758972
- 1000626221
- 9613183
- 3008520652
- 1000649241
- 3001917653
- 3018070833
- 3014560743
- 1043591
- 3010097863
- 3015429713
- 3013375723
- 3017297225
- 3007615436
- 3017621989
- 3011240418
- 3016450032
- 3006609021
- 3022082632
- 3043013796
- 3005037196
- 3006984702
- 1832894
- 3011689956
- 3007502541
- 1054236
- 9612388
- 3007218972
- 2530195
- 3015287620
- 3011786430
- 1511629
- 3027157200
- 3015526862
- 3009068676
- 3012314549
- 3010785927
- 1641302
- 3008146511
- 3019623342
- 3012494290
- 3031606416
- 3016680721
- 2087423
- 3006010416
- 3042148166
- 3031595580
- 3005083016
- 3033519
- 3007689695
- 3039396083
- 1051118
- 3027500264
- 3011678115
- 3011120089
- 3011536935
- 3008247697
- 3012027699
- 3007853907
- 3006121457
- 3011191255
- 3014663650
- 3014672091
- 1038963
- 3022114800
- 3009119999
- 3034205725
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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