510(k) K821307
- Device
- ANESTHECACHE
- Applicant
- MED-LIFE, INC.
- 510(k) number
- K821307
- Product code
- BRY
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1982-05-14
- Date received
- 1982-05-04
- Regulation
- 868.6100
- Classification name
- Cabinet, Table And Tray, Anesthesia
- Medical specialty
- Anesthesiology
- Review panel
- Anesthesiology
- 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#
- 3007123908
- 3003879246
- 3014383485
- 3005581012
- 3007573469
- 8043685
- 3011647251
- 3008559238
- 3013237609
- 3007880912
- 2031508
- 3027332478
- 3004068465
- 3009526986
- 3007218972
- 3027847726
- 9680168
- 3010097171
- 1836161
- 3037012186
- 3033433849
- 3014908171
- 3001109397
- 3010373263
- 3009567010
- 3015526491
- 3024706751
- 2024242
- 3031700059
- 3038623066
- 3007744192
- 3008881803
- 3007836437
- 3015426639
- 3003882387
- 3004604967
- 3043178571
- 3043177791
- 2030624
- 3007913191
- 1223662
- 3030488262
- 3005202235
- 3021559257
- 1218386
- 2023337
- 1924066
- 3015978022
- 3010373530
- 3030522263
- 3013408788
- 3014739961
- 3010303097
- 3013685983
- 2016493
- 9613910
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code BRY #
Legacy Summary#
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FDA Review#
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