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Lead Adaptor

FDA UDI

Class II (US FDA UDI)

by Oscor Inc.

Identity

Trade Name
Lead Adaptor FDA UDI
Generic Name
Pacing/defibrillation lead electrical adaptor FDA UDI
Device Name
Lead Adaptor FDA UDI
Model / Reference
B/IS-15 FDA UDI
Description
Lead Adaptor FDA UDI

Identifiers

Catalog Number
B/IS-15 FDA UDI
Primary DI / UDI-DI
00885672011222 FDA UDI
510(k) Number
K925168 FDA UDI
FDA Product Code
DTD FDA UDI
GMDN Term
Pacing/defibrillation lead electrical adaptor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.3620 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 15 Centimeter FDA UDI

Category: Pacing/defibrillation lead electrical adaptor

Lead Adaptor by Oscor Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pacing/defibrillation lead electrical adaptor.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oscor Inc.

Sources (1)

  • FDA UDI 1747c38a-7da4-48b4-b1ab-6b0a81176526 38 fields · synced May 30, 2026