Primary Device ID | B82110300 |
NIH Device Record Key | 4ae72eb2-9843-4f0b-a071-c42647246972 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | RevLight |
Version Model Number | 1030 |
Catalog Number | 1030 |
Company DUNS | 068492206 |
Company Name | SUBCON MANUFACTURING CORP |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | 8445066525 |
sales@rev-light.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B82110300 [Primary] |
GEX | Powered Laser Surgical Instrument |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-02-24 |
Device Publish Date | 2019-12-20 |
B82110300 | RevLight is a device that utilizes Light Emitting Diodes to provide LED light to the body. The b |
B82110290 | RevLight is a device that utilizes Light Emitting Diodes to provide LED light to the body. The b |
B82110000 | RevLight is a device that utilizes Light Emitting Diodes to provide LED light to the body. The b |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
REVLIGHT 78544801 not registered Dead/Abandoned |
ASAP Circuit 2005-01-10 |