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Lariat RS

by Atricure, Inc.

Lariat RS is a Class II device made by Atricure, Inc., cleared under FDA 510(k) K153096 on 25 Nov 2015 and listed in FDA GUDID since 30 Dec 2019 (UDI-DI 00818354017557), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K153096

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00818354017557 UDI-DI Date30 Dec 2019ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Special NumberK153096 Date25 Nov 2015DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K153096 decided 25 Nov 2015 Active
  • FDA GUDID UDI-DI 00818354017557 listed 30 Dec 2019 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K153096
  2. Listed FDA GUDID 00818354017557

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Lariat
Generic name
Suture knot pusher, single-use
Model / reference
RS
Primary DI / UDI-DI
00818354017557
510(k) Number
FDA product code
GAT, HCF
GMDN term
Suture knot pusher, single-use
Device class
Class II
Regulation number
878.5000, 878.4800
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code GAT (Suture, Nonabsorbable, Synthetic, Polyethylene).

Other devices from Atricure, Inc.

See all devices from Atricure, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)