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Flow 20

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Flow 20 FDA UDI
Generic Name
Gastrostomy tube FDA UDI
Device Name
Percutaneous Endoscopic Gastrostomy Set FDA UDI
Model / Reference
G22638 FDA UDI
Description
Percutaneous Endoscopic Gastrostomy Set FDA UDI

Identifiers

Catalog Number
FLOW-20-PULL-S FDA UDI
Primary DI / UDI-DI
00827002226388 FDA UDI
510(k) Number
K920703 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Gastrostomy tube FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Category: Gastrostomy tube

Flow 20 by Cook Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gastrostomy tube.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI 873f60fe-575b-4656-9655-7d1f686b815a 37 fields · synced Jun 8, 2026