AUTONOM

Device, Pressure Applying

AUTONOMIC EQUIPMENT SUPPLY CO,

The following data is part of a premarket notification filed by Autonomic Equipment Supply Co, with the FDA for Autonom.

Pre-market Notification Details

• Device ID: K780312
• 510k Number: K780312
• Device Name: AUTONOM
• Classification: Device, Pressure Applying
• Applicant: AUTONOMIC EQUIPMENT SUPPLY CO, 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: KNM
• CFR Regulation Number: 890.5765 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1978-02-15
• Decision Date: 1978-04-05