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ClearIt Anti-Fog Kit

FDA UDI

Class II (US FDA UDI)

by Preservation Solutions, Inc.

Identity

Trade Name
ClearIt Anti-Fog Kit FDA UDI
Generic Name
Endoscope antifog solution FDA UDI
Device Name
A sterile kit containing a 6cc vial of anti-fog solution and sponge with radiopaque marker, pack of 10 FDA UDI
Model / Reference
PS003 FDA UDI
Description
A sterile kit containing a 6cc vial of anti-fog solution and sponge with radiopaque marker, pack of 10 FDA UDI

Identifiers

Primary DI / UDI-DI
10810805000146 FDA UDI
510(k) Number
K022826 FDA UDI
FDA Product Code
OCT FDA UDI
GMDN Term
Endoscope antifog solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endoscope antifog solution

ClearIt Anti-Fog Kit by Preservation Solutions, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope antifog solution.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ecf4aac4-332c-4014-a814-50fc193742ab 35 fields · synced May 30, 2026