← Back to catalogue

LEEP PRECISION™ Generator

FDA UDI

Class II (US FDA UDI)

by CooperSurgical, Inc.

Identity

Trade Name
LEEP PRECISION™ Generator FDA UDI
Generic Name
Electrosurgical system generator FDA UDI
Device Name
LEEP PRECISION™ Generator (120 VAC) FDA UDI
Model / Reference
LP-20-120 FDA UDI
Description
LEEP PRECISION™ Generator (120 VAC) FDA UDI

Identifiers

Primary DI / UDI-DI
00888937014235 FDA UDI
510(k) Number
K963653 FDA UDI
FDA Product Code
HGI FDA UDI
GMDN Term
Electrosurgical system generator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4120 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrosurgical system generator

LEEP PRECISION™ Generator by CooperSurgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical system generator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 87288c09-fcaa-4c10-a74c-1be30eea5f20 34 fields · synced Jun 9, 2026