FDA UDI Not in Commercial Distribution 🇺🇸 United States

SQ-RX® PULSE GENERATOR

DI: 00802526562808 · Model: 1010 · CAMERON HEALTH, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SQ-RX® PULSE GENERATOR
Primary DI
00802526562808
Version / Model
1010
Company Name
CAMERON HEALTH, INC.
Labeler DUNS
017134557
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-24
Public Version
5
Public Version Date
2021-03-19
Public Version Status
Update
Public Device Record Key
6961efbb-5e1f-4d65-bcff-2ef6de95fa85
Distribution End Date
2020-06-17

Device Description

SQ-RX Pulse Generator

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LWS Implantable cardioverter defibrillator (non-CRT)

GMDN Terms

Code Name
35852 Single-chamber implantable defibrillator

Identifiers

Type ID
Primary 00802526562808

Premarket Submissions

Submission Number Supplement Number
P110042 017
P110042 020
P110042 029
P110042 038
P110042 039