ACETAMINOPHEN L3K 506-30

GUDID 00628063400034

SEKISUI DIAGNOSTICS, LLC

Acetaminophen IVD, kit, enzyme spectrophotometry

• Primary Device ID: 00628063400034
• NIH Device Record Key: 7cd533b9-81b0-4bd0-80b4-9795e2fc469a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ACETAMINOPHEN L3K
• Version Model Number: 506-30
• Catalog Number: 506-30
• Company DUNS: 966812344
• Company Name: SEKISUI DIAGNOSTICS, LLC
• 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00628063400034 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K081938

FDA Product Code

• LDP: COLORIMETRY, ACETAMINOPHEN

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: 2016-09-16

On-Brand Devices [ACETAMINOPHEN L3K]

• 00628063400034: 506-30
• 00628063400027: 506-10