FDA UDI In Commercial Distribution 🇺🇸 United States

US Hyperbaric Network

DI: G623430 · Model: 430+ · US Hyperbaric Network LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
US Hyperbaric Network
Primary DI
G623430
Version / Model
430+
Company Name
US Hyperbaric Network LLC
Labeler DUNS
096401353
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-05-02
Public Version
1
Public Version Date
2025-05-12
Public Version Status
New
Public Device Record Key
11e142e4-acbc-4476-b79e-ccaeeb7e9cdd
Distribution End Date
2028-05-02

Device Description

The Portable Hyperbaric Chamber Revitalair® 430+ is a hyperbaric semi-rigid chamber for low pressures (operating at pressures of no greater than 1.5 atmospheres absolute (ATA)). The operational design pressure of a hyperbaric chamber that encloses a human within its pressure boundary falls within the scope of the American Society of Mechanical Engineers Pressure Vessels Human Occupancy 1 (ASME PVHO 1-2012).

Device Characteristics

Single Use
No
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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
CBF Chamber, Hyperbaric

GMDN Terms

Code Name
12061 Hyperbaric chamber, stationary

Identifiers

Type ID
Primary G623430

Premarket Submissions

Submission Number Supplement Number
K220290 000