THERAPlus

GUDID 00049696738132

TheraPlus Digital thermometer

FOURSTAR GROUP INC.

Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer Intermittent electronic patient thermometer

• Primary Device ID: 00049696738132
• NIH Device Record Key: 9e1d5f29-eeb8-4be2-a904-8ddbdd31ea84
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: THERAPlus
• Version Model Number: 11012340F
• Company DUNS: 656091279
• Company Name: FOURSTAR GROUP 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: true
• Lot Batch: true
• Serial Number: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00049696738132 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K102718

FDA Product Code

• FLL: Thermometer, Electronic, Clinical

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-06-28
• Device Publish Date: 2021-06-18

On-Brand Devices [THERAPlus]

• 00049696731621: Theraplus INFRARED FOREHEAD THERMOMETER
• 00049696731379: Theraplus DIGITAL THERMOMETER
• 00049696738132: TheraPlus Digital thermometer
• 00049696739351: TheraPlus CHILDRENS CHARACTER THERMOMETER
• 00049696739795: TheraPlus CHILDRENS CHARACTER THERMOMETER