Identity
- Trade Name
- Lead Adapter Cable FDA UDI
- Generic Name
- Electrical-only medical device connection cable, reusable FDA UDI
- Device Name
- Lead Adapter Cable, 1x For use with Model B31040 lead test cable FDA UDI
- Model / Reference
- MT-LA-04-00823 FDA UDI
- Description
- Lead Adapter Cable, 1x For use with Model B31040 lead test cable FDA UDI
Identifiers
- Catalog Number
- MT-LA-04 FDA UDI
- Primary DI / UDI-DI
- 00873263008232 FDA UDI
- 510(k) Number
- K183123 FDA UDI
- FDA Product Code
- GZL FDA UDI
- GMDN Term
- Electrical-only medical device connection cable, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1330 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Electrical-only medical device connection cable, reusable
Lead Adapter Cable by Fhc, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Electrical-only medical device connection cable, reusable.
- Unimed — Unimed Medical Supplies, Inc. · Class II
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- Unimed — Unimed Medical Supplies, Inc. · Class II
- Symmetry Olsen — Olsen Medical · Class II
- Connection Cable — Shenzhen Keborui Electronics Co., Ltd · Class I
- TC-HEART LUNG DIN INTFC CA STOCKET — ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. · Class II
- MICTEC CONNECTION CABLE — SONTEC INSTRUMENTS, INC. · Class II
- ECG Cable — Edan Instruments,Inc. · Class I
Cleared under the same submission
K183123 also covers:
- Guideline 4000 5.0™ 3m Interface Cable — FHC, INC.
- Guideline 4000 5.0™ Interface — FHC, INC.
- Guideline 4000 5.0™ LF Interface — FHC, INC.
- Guideline 4000 5.0™ Motor & Encoder — FHC, INC.
- Guideline 4000 5.0™ microTargeting™ Controller Card — FHC, INC.
- Guideline 4000 5.0™ microTargeting™ Interface Card — FHC, INC.
- Guideline 4000™ 5.0 — FHC, INC.
- Guideline 4000™ 5.0 — FHC, INC.
- Guideline 4000™ 5.0 — FHC, INC.
- Guideline 4000™ 5.0 — FHC, INC.
- Guideline 4000™ 5.0 Accessory — FHC, INC.
- Resident Expert Kinetic Testing Motion Detector — FHC, INC.
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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Fhc, Inc.
Sources (1)
- FDA UDI 63fcd660-ba66-44c0-9e4e-367b0a46b8b5 36 fields · synced Jun 8, 2026