| Primary Device ID | B24523001B1 |
| NIH Device Record Key | 4e62dbca-30ff-40c2-b2b7-9939d9cbe8c5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SSCOR/board |
| Version Model Number | 23001B |
| Company DUNS | 131254971 |
| Company Name | SSCOR, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B24523001B1 [Primary] |
| GCX | Apparatus, Suction, Operating-Room, Wall Vacuum Powered |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-08-23 |
| Device Publish Date | 2016-09-16 |
| B245250001 | Onboard Suction Device |
| B24523001WCKK1 | Onboard Suction Device |
| B24523001WCK15 | Onboard Suction Device |
| B24523001WC1 | Onboard Suction Device |
| B24523001PLC1 | Onboard Suction Device |
| B24523001B1 | Onboard Suction Device |
| B245230011 | Onboard Suction Device |
| B245225001 | Onboard Suction Device |
| B24522020LDR12 | Onboard Suction Device |
| B24522000RRC15 | Onboard Suction Device |
| B24522000PLC1 | Onboard Suction Device |
| B24522000GIFA1 | Onboard Suction Device |
| B24522000BRAUN1 | Onboard Suction Device |
| B245220001 | Onboard Suction Device |