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Dcx

FDA UDI

Class II (US FDA UDI)

by Osko, Inc.

Identity

Trade Name
DCX FDA UDI
Generic Name
Stationary basic diagnostic x-ray system, analogue FDA UDI
Device Name
Stationary X-Ray System FDA UDI
Model / Reference
DCX FDA UDI
Description
Stationary X-Ray System FDA UDI

Identifiers

Primary DI / UDI-DI
00869126000468 FDA UDI
510(k) Number
K150663 FDA UDI
FDA Product Code
KPR FDA UDI
GMDN Term
Stationary basic diagnostic x-ray system, analogue FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1680 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

No

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: Stationary basic diagnostic x-ray system, analogue

Dcx by Osko, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stationary basic diagnostic x-ray system, analogue.

Cleared under the same submission

K150663 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Osko, Inc.

Sources (1)

  • FDA UDI bcc7713b-6697-4b33-80b8-0b4fcd95022b 35 fields · synced Jun 8, 2026