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Infrared And Blue Light Filter Unit

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
INFRARED AND BLUE LIGHT FILTER UNIT FDA UDI
Generic Name
Surgical microscope video camera filter switch FDA UDI
Model / Reference
MAJ-2308 FDA UDI

Identifiers

Catalog Number
N5769940 FDA UDI
Primary DI / UDI-DI
04953170396113 FDA UDI
510(k) Number
K190772 FDA UDI
FDA Product Code
IZI FDA UDI
EPT FDA UDI
GMDN Term
Surgical microscope video camera filter switch FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1600 FDA UDI
878.4700 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: Surgical microscope video camera filter switch

Infrared And Blue Light Filter Unit by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical microscope video camera filter switch.

Cleared under the same submission

K190772 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Olympus Medical Systems Corporation

Sources (1)

  • FDA UDI 261b14c0-cd5e-4fc7-a162-3e9f50c829e3 35 fields · synced May 30, 2026