TheraClear - THERAVANT CORPORATION

Duns Number:927989959

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More Product Details

Catalog Number

30TC073

Brand Name

TheraClear

Version/Model Number

30TC073AA00

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

ONF

Product Code Name

Powered Light Based Non-Laser Surgical Instrument With Thermal Effect

Device Record Status

Public Device Record Key

e4c08ada-05a7-41b2-b67c-6a5a2aac68c3

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 19, 2016

Additional Identifiers

Package DI Number

B30530TC0731

Quantity per Package

20

Contains DI Package

B30530TC0730

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box

"THERAVANT CORPORATION" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 1