← Back to catalogue

Panosol II Cabinet

FDA UDI

Class II (US FDA UDI)

by National Biological Corp.

Identity

Trade Name
Panosol II Cabinet FDA UDI
Generic Name
Ultraviolet phototherapy unit, professional FDA UDI
Model / Reference
UVB-651 FDA UDI

Identifiers

Primary DI / UDI-DI
00816878020855 FDA UDI
510(k) Number
K827890 FDA UDI
FDA Product Code
FTC FDA UDI
GMDN Term
Ultraviolet phototherapy unit, professional FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4630 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ultraviolet phototherapy unit, professionalUltraviolet phototherapy unit, home-use

Panosol II Cabinet by National Biological Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ultraviolet phototherapy unit, home-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 253189b9-eb63-4d47-b2ae-1d7ffc1508a9 34 fields · synced Jun 8, 2026