ARGYLE INDWELL FEEDING TUBE

Tubes, Gastrointestinal (and Accessories)

SHERWOOD MEDICAL CO.

The following data is part of a premarket notification filed by Sherwood Medical Co. with the FDA for Argyle Indwell Feeding Tube.

Pre-market Notification Details

• Device ID: K820442
• 510k Number: K820442
• Device Name: ARGYLE INDWELL FEEDING TUBE
• Classification: Tubes, Gastrointestinal (and Accessories)
• Applicant: SHERWOOD MEDICAL CO. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: KNT
• CFR Regulation Number: 876.5980 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1982-02-18
• Decision Date: 1982-03-10

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
40884521003836	K820442	000
40884521003812	K820442	000