FDA UDI Not in Commercial Distribution 🇺🇸 United States

Control Syringe

DI: 00886333207312 · Model: 193239 · ARGON MEDICAL DEVICES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Control Syringe
Primary DI
00886333207312
Version / Model
193239
Catalog Number
193239
Company Name
ARGON MEDICAL DEVICES, INC.
Labeler DUNS
140727624
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-09
Public Version
6
Public Version Date
2026-04-17
Public Version Status
Update
Public Device Record Key
e3a6a9fc-695a-4df1-a13b-65ee40b1c080
Distribution End Date
2024-04-16

Device Description

12cc Soft Touch Control Syringe FG/PP/RA w/Reservoir

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
IZI System, X-Ray, Angiographic

GMDN Terms

Code Name
47017 General-purpose syringe, single-use

Identifiers

Type ID
Package 20886333207316
Primary 00886333207312

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K911732 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 12cc