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Sc Honkytonk

FDA UDI

Class II (US FDA UDI)

by Sino Medical Sciences Technology Inc.

Identity

Trade Name
SC HONKYTONK FDA UDI
Generic Name
Coronary angioplasty balloon catheter, basic FDA UDI
Device Name
The SC HONKYTONK™ PTCA Balloon Dilatation Catheter is indicated for the balloon catheter dilatation of the stenotic portion of a coronary artery or bypass graft stenosis for the purpose of improving myocardial perfusion. FDA UDI
Model / Reference
SCB-1.50-15-RX FDA UDI
Description
The SC HONKYTONK™ PTCA Balloon Dilatation Catheter is indicated for the balloon catheter dilatation of the stenotic portion of a coronary artery or bypass graft stenosis for the purpose of improving myocardial perfusion. FDA UDI

Identifiers

Primary DI / UDI-DI
06948546214052 FDA UDI
510(k) Number
K223022 FDA UDI
FDA Product Code
LOX FDA UDI
GMDN Term
Coronary angioplasty balloon catheter, basic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5100 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Coronary angioplasty balloon catheter, basic

Sc Honkytonk by Sino Medical Sciences Technology Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coronary angioplasty balloon catheter, basic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 468b012e-1cd2-4ed6-8061-451958031124 35 fields · synced May 30, 2026