Lariat RS

FDA UDI

Class I (US FDA UDI)

by Atricure, Inc.

Identity

Trade Name: Lariat RS FDA UDI
Generic Name: Suture knot pusher, single-use FDA UDI
Device Name: LARIAT RS Suture Delivery Device, 45mm FDA UDI
Model / Reference: 30-06 FDA UDI
Description: LARIAT RS Suture Delivery Device, 45mm FDA UDI

Identifiers

Catalog Number: FG-0028-02 FDA UDI
Primary DI / UDI-DI: 10840143909443 FDA UDI
510(k) Number: K153096 FDA UDI
FDA Product Code: HCF FDA UDI
GAT FDA UDI
GMDN Term: Suture knot pusher, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
878.5000 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Safe FDA UDI

Dimensions & Sizes

Size: Length — 45 Millimeter FDA UDI

Category: Suture knot pusher, single-use

Lariat RS by Atricure, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suture knot pusher, single-use.

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FAST-FIX — Smith & Nephew, Inc. · Class I
FAST-FIX — Smith & Nephew, Inc. · Class I
RapidLink — Hangzhou Rejoin Mastin Medical Device Co., Ltd. · Class I

Cleared under the same submission

K153096 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Atricure, Inc.

Sources (1)

FDA UDI f205d678-cdb9-4076-b2eb-79316a78f123 38 fields · synced May 30, 2026