Quasar MD Blue Pink DPA-022-PK

GUDID 00851478007097

This light therapy prescription-strength powerhouse banishes blemishes at their core with a larger treatment head bringing the dermatologist into your living room. Unlike other treatments such as drying topical products, the results achieved with your Quasar MD Blue will endure, lasting weeks and months only requiring occasional maintenance treatments

QUASAR BIO-TECH INC.

Blue/red/infrared phototherapy lamp

• Primary Device ID: 00851478007097
• NIH Device Record Key: 71b42360-b604-41e5-bbb6-0c839285a21c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Quasar MD Blue Pink
• Version Model Number: DPA-022-PK
• Catalog Number: DPA-022-PK
• Company DUNS: 849862912
• Company Name: QUASAR BIO-TECH INC.
• 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: true
• Serial Number: false
• Manufacturing Date: true
• 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: true

Customer Support Contacts

• Phone: 941-306-5812
• Email: denette@quasarbiotech.com
• Phone: 941-306-5812
• Email: denette@quasarbiotech.com
• Phone: 941-306-5812
• Email: denette@quasarbiotech.com
• Phone: 941-306-5812
• Email: denette@quasarbiotech.com
• Phone: 941-306-5812
• Email: denette@quasarbiotech.com
• Phone: 941-306-5812
• Email: denette@quasarbiotech.com
• Phone: 941-306-5812
• Email: denette@quasarbiotech.com
• Phone: 941-306-5812
• Email: denette@quasarbiotech.com
• Phone: 941-306-5812
• Email: denette@quasarbiotech.com
• Phone: 941-306-5812
• Email: denette@quasarbiotech.com
• Phone: 941-306-5812
• Email: denette@quasarbiotech.com
• Phone: 941-306-5812
• Email: denette@quasarbiotech.com
• Phone: 941-306-5812
• Email: denette@quasarbiotech.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00851478007097 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K093963

FDA Product Code

• OLP: Over-The-Counter Powered Light Based Laser For Acne

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-19

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