Advanced Chiropractic Equipment LLC

GUDID 00860011173649

HILL LABORATORIES CO.

Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered Examination/treatment table, line-powered

• Primary Device ID: 00860011173649
• NIH Device Record Key: 914b8350-8303-490f-9202-866724772bbb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Advanced Chiropractic Equipment LLC
• Version Model Number: ACR Table
• Company DUNS: 002326585
• Company Name: HILL LABORATORIES CO.
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860011173649 [Primary]

FDA Product Code

• INQ: Table, Powered

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: 2023-10-31
• Device Publish Date: 2023-10-23

Devices Manufactured by HILL LABORATORIES CO.

• 00850058158143 - The SAVE Program: 2024-03-19
• 00850058158006 - HA90R: 2023-11-01
• 00850058158051 - HA90P: 2023-11-01
• 00850058158068 - HA90PH: 2023-11-01
• 00850058158075 - HA90PT: 2023-11-01
• 00850058158082 - HA90V: 2023-11-01
• 00850058158099 - HA90W: 2023-11-01
• 00850058158105 - HI-LO: 2023-11-01