ZERO-G

Cushion, Flotation

STERIDYNE CORP.

The following data is part of a premarket notification filed by Steridyne Corp. with the FDA for Zero-g.

Pre-market Notification Details

• Device ID: K842120
• 510k Number: K842120
• Device Name: ZERO-G
• Classification: Cushion, Flotation
• Applicant: STERIDYNE CORP. 4221 Richmond Rd., N.W. Walker, MI 49534
• Product Code: KIC
• CFR Regulation Number: 890.3175 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1984-05-29
• Decision Date: 1984-06-08