JUHN TYM-TAP

Container, Specimen, Sterile

XOMED, INC.

The following data is part of a premarket notification filed by Xomed, Inc. with the FDA for Juhn Tym-tap.

Pre-market Notification Details

• Device ID: K790915
• 510k Number: K790915
• Device Name: JUHN TYM-TAP
• Classification: Container, Specimen, Sterile
• Applicant: XOMED, INC. 1318 LONEDELL RD. Arnold, MO 63010
• Product Code: FMH
• CFR Regulation Number: 864.3250 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1979-05-14
• Decision Date: 1979-06-27

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
20681490041762	K790915	000
00763000040024	K790915	000