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Rho

FDA UDI

Class II (US FDA UDI)

by 16 Bit, Inc.

Identity

Trade Name
Rho FDA UDI
Generic Name
X-ray image interpretive software FDA UDI
Device Name
Rho radiology software for opportunistic evaluation of low bone mineral density. FDA UDI
Model / Reference
Rho FDA UDI
Description
Rho radiology software for opportunistic evaluation of low bone mineral density. FDA UDI

Identifiers

Primary DI / UDI-DI
06287194090220 FDA UDI
510(k) Number
FDA Product Code
SAO FDA UDI
GMDN Term
X-ray image interpretive software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1171 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: X-ray image interpretive software

Rho by 16 Bit, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as X-ray image interpretive software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
16 Bit, Inc.

Sources (1)

  • FDA UDI 980f8d2d-fd1a-4cde-acbe-e215a2c44a9b 34 fields · synced Jun 8, 2026