PROCAST

Bandage, Cast

MEDICAL SPECIALTIES, INC.

The following data is part of a premarket notification filed by Medical Specialties, Inc. with the FDA for Procast.

Pre-market Notification Details

• Device ID: K791831
• 510k Number: K791831
• Device Name: PROCAST
• Classification: Bandage, Cast
• Applicant: MEDICAL SPECIALTIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: ITG
• CFR Regulation Number: 890.3025 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1979-09-18
• Decision Date: 1979-09-24