510(k) K791176
- Device
- 3M COLD/HOT WATER BAG AND WRAP
- Applicant
- 3M COMPANY
- 510(k) number
- K791176
- Product code
- FPF
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1979-07-30
- Date received
- 1979-06-25
- Regulation
- 880.6085
- Classification name
- Bottle, Hot/cold Water
- Medical specialty
- General Hospital
- Review panel
- General Hospital
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Address
- 8124 Pacific Ave. White City OR US 97503 97503
FDA Registration Numbers#
- 9680411
- 3015173212
- 3036779619
- 3012466243
- 3043654665
- 3009308092
- 1000328618
- 3003965134
- 3010374920
- 2432177
- 3006113277
- 3030412032
- 3009648765
- 8043782
- 1422443
- 3012316249
- 2081040
- 3005327291
- 3012428275
- 3016450032
- 3034669683
- 2183416
- 3042256682
- 1039131
- 3009068676
- 3016075711
- 3004122598
- 1063974
- 3015220641
- 3006542501
- 3005951403
- 3015745029
- 3006897996
- 8043965
- 3004024088
- 3010409218
- 1417592
- 3014982318
- 3017417635
- 3038195661
- 3008412545
- 9710020
- 3005632310
- 3016170451
- 3022082632
- 3008997160
- 3006806517
- 1036836
- 9613910
- 3000099306
- 3008808082
- 3010967704
- 3004365956
- 3013839458
- 3012314549
- 3036893546
- 3042896810
- 3004824601
- 3011137372
- 3021963363
- 3011118556
- 3041928150
- 8022890
- 2028411
- 3009974348
- 3001650535
- 3005273623
- 9611024
- 3010041511
- 3007703436
- 8043685
- 3011680766
Source Documents#
510(k) summary PDF not indicated by FDA
Legacy Summary#
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FDA Review#
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