FLEXPLUG

Plug, Punctum

EAGLE VISION, INC.

The following data is part of a premarket notification filed by Eagle Vision, Inc. with the FDA for Flexplug.

Pre-market Notification Details

• Device ID: K991130
• 510k Number: K991130
• Device Name: FLEXPLUG
• Classification: Plug, Punctum
• Applicant: EAGLE VISION, INC. 6263 POPLAR AVENUE, SUITE 650 Memphis, TN 38119
• Contact: Jim Barley
• Correspondent: Jim Barley; EAGLE VISION, INC. 6263 POPLAR AVENUE, SUITE 650 Memphis, TN 38119
• Product Code: LZU
• CFR Regulation Number: 510(k) Premarket Notification [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Special
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1999-04-02
• Decision Date: 1999-04-20

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00841668114391	K991130	000
00841668114506	K991130	000
00841668114513	K991130	000
00841668114520	K991130	000
00841668114537	K991130	000
00841668114544	K991130	000
00841668114551	K991130	000
00841668114568	K991130	000
00841668114575	K991130	000
00841668114490	K991130	000
00841668114483	K991130	000
00841668114407	K991130	000
00841668114414	K991130	000
00841668114421	K991130	000
00841668114438	K991130	000
00841668114445	K991130	000
00841668114452	K991130	000
00841668114469	K991130	000
00841668114476	K991130	000
00841668114582	K991130	000
00841668114599	K991130	000
00841668114605	K991130	000
00841668115015	K991130	000
00841668115022	K991130	000
00841668115039	K991130	000
00841668115046	K991130	000
00841668115053	K991130	000
00841668115060	K991130	000
00841668115077	K991130	000
00841668115084	K991130	000
00841668115008	K991130	000
00841668114995	K991130	000
00841668114612	K991130	000
00841668114629	K991130	000
00841668114636	K991130	000
00841668114643	K991130	000
00841668114957	K991130	000
00841668114964	K991130	000
00841668114971	K991130	000
00841668114988	K991130	000
00841668115091	K991130	000