SLICK SET

Tube, Tracheal (w/wo Connector)

POLAMEDCO, INC.

The following data is part of a premarket notification filed by Polamedco, Inc. with the FDA for Slick Set.

Pre-market Notification Details

• Device ID: K780900
• 510k Number: K780900
• Device Name: SLICK SET
• Classification: Tube, Tracheal (w/wo Connector)
• Applicant: POLAMEDCO, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: BTR
• CFR Regulation Number: 868.5730 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1978-05-15
• Decision Date: 1978-07-17

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
34026704647041	K780900	000
44026704319532	K780900	000
24026704319545	K780900	000
24026704319569	K780900	000
24026704319576	K780900	000
24026704319583	K780900	000
44026704319594	K780900	000
44026704319600	K780900	000
44026704319617	K780900	000
24026704319620	K780900	000
24026704319552	K780900	000
24026704644876	K780900	000
24026704644883	K780900	000
34026704644897	K780900	000
24026704644920	K780900	000
24026704644937	K780900	000
24026704644944	K780900	000
24026704647037	K780900	000
44026704319631	K780900	000