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Alinity

FDA UDI

Class U (US FDA UDI)

by Abbott Laboratories, Inc.

Identity

Trade Name
Alinity FDA UDI
Generic Name
Phencyclidine (PCP) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
Alinity c Phencyclidine Reagent Kit 400 Tests FDA UDI
Model / Reference
09P6620 FDA UDI
Description
Alinity c Phencyclidine Reagent Kit 400 Tests FDA UDI

Identifiers

Catalog Number
09P6620 FDA UDI
Primary DI / UDI-DI
00380740165291 FDA UDI
510(k) Number
K935320 FDA UDI
FDA Product Code
LCM FDA UDI
GMDN Term
Phencyclidine (PCP) IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
U 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

Yes

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: Phencyclidine (PCP) IVD, kit, enzyme immunoassay (EIA)

Alinity by Abbott Laboratories, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Phencyclidine (PCP) IVD, kit, enzyme immunoassay (EIA).

Cleared under the same submission

K935320 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cc669d70-abe0-4f29-9873-eeb3c32cbc81 37 fields · synced May 31, 2026